Canonical Allele Identifier: PA2828777168
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711752

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Gly426Glu
CA369588919
NM_001378470.1:c.1277G>A