Canonical Allele Identifier: PA2580233078
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711785
ClinVar RCV Id: RCV002293330

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361187.1:p.Gln496Leu
CA369588944
NM_001374258.1:c.1487A>T