Canonical Allele Identifier: PA2828777004
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Gly231Arg
CA261666
NM_001378470.1:c.691G>C