Canonical Allele Identifier: PA2828776682
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 41446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Lys579Gln
CA215454
NM_001378469.1:c.1735A>C