Canonical Allele Identifier: PA2828779064
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_001365402.1:p.Gly412Arg
CA10602955
NM_001378473.1:c.1234G>C
CA16042578
NM_001378473.1:c.1234G>A