Canonical Allele Identifier: PA2828780382
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_001365404.1:p.Gly376Arg
CA10602955
NM_001378475.1:c.1126G>C
CA16042578
NM_001378475.1:c.1126G>A