Canonical Allele Identifier: PA2828778519
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13976

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Lys447Glu
CA279972
NM_001378472.1:c.1339A>G