Allele Registry

Canonical Allele Identifier: PA2829576203

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV002012209

ClinVar Variation:

1448655

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Ala189Gly	CA5976702 NM_005055.5:c.566C>G