Allele Registry

Canonical Allele Identifier: PA2827111188

Gene: RPS19 HGNC NCBI

ClinVar RCV:

RCV000413436

RCV001066690

RCV002374616

RCV002375652

RCV003168598

ClinVar Variation:

372494

860401

1736908

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308413.1:p.Met1Ile