Canonical Allele Identifier: PA2828777359
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 41446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365399.1:p.Lys567Gln
CA215454
NM_001378470.1:c.1699A>C