Canonical Allele Identifier: PA2828780357
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711780
ClinVar RCV Id: RCV002293325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Asp357Tyr
CA369589028
NM_001378475.1:c.1069G>T