Canonical Allele Identifier: PA2827883513
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341538.1:p.Val600Gly
CA281998
NM_001354609.2:c.1799T>G