Allele Registry

Canonical Allele Identifier: PA2827111218

Gene: RPS19 HGNC NCBI

ClinVar RCV:

RCV000358661

RCV001094592

RCV001564337

RCV001820988

ClinVar Variation:

329392

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308413.1:p.Lys23Arg	CA9465269 NM_001321484.1:c.68A>G