Canonical Allele Identifier: PA279980
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_004324.2:p.Gly534Arg
CA279978
NM_004333.6:c.1600G>C