Canonical Allele Identifier: PA2828776679
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40390

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Lys579Ile
CA282001
NM_001378469.1:c.1736A>T