Canonical Allele Identifier: PA2828778528
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Leu453Phe
CA281980
NM_001378472.1:c.1357C>T