Allele Registry

Canonical Allele Identifier: PA916025063

Gene: RPS19 HGNC NCBI

ClinVar Allele:

21353

ClinVar RCV:

RCV000033183

RCV000497714

RCV001065746

RCV003415668

ClinVar Variation:

6314

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308413.1:p.Arg62Trp	CA130763 NM_001321484.1:c.184C>T