Canonical Allele Identifier: PA2828776567
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 40375

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Leu483Phe
CA281980
NM_001378469.1:c.1447C>T