Canonical Allele Identifier: PA261619
Gene: RAF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 40601

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002871.1:p.Ser259Thr
CA261617
NM_002880.4:c.775T>A