Canonical Allele Identifier: PA2828779949
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365403.1:p.Val600Gly
CA281998
NM_001378474.1:c.1799T>G