Canonical Allele Identifier: PA2828778889
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 44832

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Gly213Arg
CA261666
NM_001378473.1:c.637G>C