Canonical Allele Identifier: PA2828775286
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40387

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365396.1:p.Gly599Val
CA220161
NM_001378467.1:c.1796G>T