Canonical Allele Identifier: PA2828776329
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13965

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365398.1:p.Ala246Pro
CA279968
NM_001378469.1:c.736G>C