Canonical Allele Identifier: PA282000
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40389
ClinVar RCV Id: RCV000208774 RCV000433794 RCV000798913 RCV001354831
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Val600Gly
CA281998
NM_004333.6:c.1799T>G