Canonical Allele Identifier: PA2828777197
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13970
ClinVar Variation Id: 177775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Gly435Arg
CA123653
NM_001378470.1:c.1303G>C
CA180746
NM_001378470.1:c.1303G>A