Canonical Allele Identifier: PA2828777269
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13980
ClinVar RCV Id: RCV000015014 RCV000208775 RCV000623633 RCV000779634 RCV001257953
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Gly500Arg
CA279978
NM_001378470.1:c.1498G>C