Canonical Allele Identifier: PA2828778581
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 13979

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365401.1:p.Asn529Asp
CA279976
NM_001378472.1:c.1585A>G