Canonical Allele Identifier: PA1139743259
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44801
ClinVar Variation Id: 2501901
ClinVar RCV Id: RCV003228320

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Gly506Arg
CA135079
NM_001374258.1:c.1516G>A
CA168090546
NM_001374258.1:c.1516G>C