Canonical Allele Identifier: PA281997
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004324.2:p.Thr599Ile
CA281995
NM_004333.6:c.1796C>T