Canonical Allele Identifier: PA1139744760
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Gly268Arg
CA261666
NM_001378467.1:c.802G>C