Canonical Allele Identifier: PA2828475058
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361173.1:p.Val640Gly
CA281998
NM_001374244.1:c.1919T>G