Canonical Allele Identifier: PA2828776590
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13980

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Gly512Arg
CA279978
NM_001378469.1:c.1534G>C