Allele Registry

Canonical Allele Identifier: PA658667076

Gene: RAPSN HGNC NCBI

ClinVar Variation Id: 476117

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Asn394Ser	CA5976460 NM_005055.5:c.1181A>G