Canonical Allele Identifier: PA1139743279
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Cys572Tyr
CA175337
NM_001374258.1:c.1715G>A