Canonical Allele Identifier: PA2828775304
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40389
ClinVar RCV Id: RCV000208774 RCV000433794 RCV000798913 RCV001354831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Val603Gly
CA281998
NM_001378467.1:c.1808T>G