Allele Registry

Canonical Allele Identifier: PA2827111165

Gene: RPS19 HGNC NCBI

ClinVar RCV:

RCV000033189

RCV002512845

ClinVar Variation:

6320

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308412.1:p.Gly127Glu	CA130769 NM_001321483.1:c.380G>A