Allele Registry

Canonical Allele Identifier: PA2741821542

Gene: RPS28 HGNC NCBI

ClinVar RCV:

RCV003740317

ClinVar Variation:

2916205

HGVS (amino-acid)	Matching Registered Transcripts
NP_001022.1:p.Thr3Ala	CA9155124 NM_001031.5:c.7A>G