Allele Registry

Canonical Allele Identifier: PA163478

Gene: RPS29 HGNC NCBI

ClinVar RCV:

RCV000128850

ClinVar Variation:

140738

HGVS (amino-acid)	Matching Registered Transcripts
NP_001025172.1:p.Ile31Phe	CA163477 NM_001030001.4:c.91A>T