Canonical Allele Identifier: PA261668
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Gly265Arg
CA261666
NM_004333.6:c.793G>C