Allele Registry

Canonical Allele Identifier: PA2827608345

Gene: RPS29 HGNC NCBI

ClinVar RCV:

RCV000128850

ClinVar Variation:

140738

HGVS (amino-acid)	Matching Registered Transcripts
NP_001338304.1:p.Ile28Phe	CA163477 NM_001351375.2:c.82A>T