Allele Registry

Canonical Allele Identifier: PA2827608352

Gene: RPS29 HGNC NCBI

ClinVar Allele:

150452

ClinVar RCV:

RCV000128851

ClinVar Variation:

140739

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338304.1:p.Ile47Thr	CA163479 NM_001351375.2:c.140T>C