Canonical Allele Identifier: PA2828779229
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40389

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365402.1:p.Val548Gly
CA281998
NM_001378473.1:c.1643T>G