Allele Registry

Canonical Allele Identifier: PA916071597

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008522

RCV001231489

RCV003460443

ClinVar Variation:

8056

HGVS (amino-acid)	Matching Registered Transcripts
NP_116034.2:p.Glu162Lys	CA119258 NM_032645.5:c.484G>A