Canonical Allele Identifier: PA2827883321
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711785
ClinVar RCV Id: RCV002293330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Gln456Leu
CA369588944
NM_001354609.2:c.1367A>T