Allele Registry

Canonical Allele Identifier: PA113367

Gene: RPS19 HGNC NCBI

ClinVar RCV:

RCV000471188

RCV001331478

RCV001507957

RCV001843501

ClinVar Variation:

242753

HGVS (amino-acid)	Matching Registered Transcripts
NP_001013.1:p.Thr55Met	CA045548 NM_001022.3:c.164C>T