Canonical Allele Identifier: PA2828775837
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13962
ClinVar RCV Id: RCV000014995

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365397.1:p.Arg462Ile
CA250632
NM_001378468.1:c.1385G>T