Canonical Allele Identifier: PA2828780207
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Gly177Arg
CA261666
NM_001378475.1:c.529G>C