Allele Registry

Canonical Allele Identifier: PA916071627

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008525

ClinVar Variation:

8059

HGVS (amino-acid)	Matching Registered Transcripts
NP_116034.2:p.Ala189Val	CA119260 NM_032645.5:c.566C>T