Allele Registry

Canonical Allele Identifier: PA891866110

Gene: RPS19 HGNC NCBI

ClinVar RCV:

RCV000033185

ClinVar Variation:

6316

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308414.1:p.Glu88Val	CA130766 NM_001321485.1:c.263A>T