Allele Registry

Canonical Allele Identifier: PA2827111202

Gene: RPS19 HGNC NCBI

ClinVar RCV:

RCV000482973

ClinVar Variation:

242804

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308413.1:p.Val15Phe	CA045535 NM_001321484.1:c.43G>T