Canonical Allele Identifier: PA2828775137
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 279992
ClinVar RCV Id: RCV000304268
ClinVar Variation Id: 372572

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Gly467Arg
CA10602955
NM_001378467.1:c.1399G>C
CA16042578
NM_001378467.1:c.1399G>A