Allele Registry

Canonical Allele Identifier: PA891866111

Gene: RPS19 HGNC NCBI

ClinVar Allele:

21352

ClinVar RCV:

RCV000033182

RCV000272977

RCV002433445

ClinVar Variation:

6313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001308414.1:p.Pro98Leu	CA130761 NM_001321485.1:c.293C>T