Canonical Allele Identifier: PA261622
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 44631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002871.1:p.Arg256Gly
CA261620
NM_002880.4:c.766A>G