Allele Registry

Canonical Allele Identifier: PA645500786

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000269370

RCV000366609

RCV000810152

RCV001276398

RCV002480112

ClinVar Variation:

304980

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Val138Ile	CA5976748 NM_005055.5:c.412G>A