Allele Registry

Canonical Allele Identifier: PA645500896

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000261059

RCV000316244

RCV000525112

RCV001274409

RCV001531730

RCV004537718

ClinVar Variation:

304973

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Ser274Asn	CA5976611 NM_005055.5:c.821G>A