| missense mutation | Q2656896 |
| P3329 | CIViC variant ID | 604 |
| P6861 | dbSNP Reference SNP number | rs121913492 |
| P3331 | HGVS nomenclature | ENST00000286548.4:c.626A>C |
| NC_000009.11:g.80409488T>G | ||
| NM_002072.4:c.626A>C | ||
| NP_002063.2:p.Gln209Pro |
| P3433 | biological variant of | GNAQ | Q18026236 |
| P1057 | chromosome | human chromosome 9 | Q840604 |
| P645 | genomic end | 80409488 | |
| P644 | genomic start | 80409488 | |
| P3355 | negative therapeutic predictor for | plx-4720 | Q27088418 |
| vemurafenib | Q423111 |
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