Allele Registry

Canonical Allele Identifier: PA2827021629

Gene: CNPY3 HGNC NCBI

ClinVar RCV:

RCV004207187

ClinVar Variation:

2367744

HGVS (amino-acid)	Matching Registered Transcripts
NP_001305776.1:p.Leu23Pro	CA138246014 NM_001318847.2:c.68T>C