Canonical Allele Identifier: PA2828779077
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13970
ClinVar Variation Id: 177775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Gly417Arg
CA123653
NM_001378473.1:c.1249G>C
CA180746
NM_001378473.1:c.1249G>A