Canonical Allele Identifier: PA175339
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40380

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Cys532Tyr
CA175337
NM_004333.6:c.1595G>A