Canonical Allele Identifier: PA2828780562
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 41446

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365404.1:p.Lys513Gln
CA215454
NM_001378475.1:c.1537A>C