Canonical Allele Identifier: PA2828775226
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Gly537Arg
CA279978
NM_001378467.1:c.1609G>C