Canonical Allele Identifier: PA281967
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40365
ClinVar RCV Id: RCV000824917 RCV001807745
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Gly464Ala
CA281965
NM_004333.6:c.1391G>C