Canonical Allele Identifier: PA2828775863
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13970
ClinVar Variation Id: 177775

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Gly469Arg
CA123653
NM_001378468.1:c.1405G>C
CA180746
NM_001378468.1:c.1405G>A