Allele Registry

Canonical Allele Identifier: PA916071687

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000553703

RCV001274410

RCV001556490

ClinVar Variation:

476125

HGVS (amino-acid)	Matching Registered Transcripts
NP_116034.2:p.Arg259His	CA5976642 NM_032645.5:c.776G>A