Canonical Allele Identifier: PA2828776558
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13976
ClinVar RCV Id: RCV000015010 RCV000207517 RCV000779848 RCV001813210
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Lys477Glu
CA279972
NM_001378469.1:c.1429A>G