Canonical Allele Identifier: PA2828776986
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Ala212Pro
CA279968
NM_001378470.1:c.634G>C