Allele Registry

Canonical Allele Identifier: PA645500821

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000432123

RCV001731679

RCV002466497

RCV002519529

ClinVar Variation:

381702

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Glu147Lys	CA5976743 NM_005055.5:c.439G>A