Allele Registry

Canonical Allele Identifier: PA2830086296

Gene: RAPSN HGNC NCBI

ClinVar Variation Id: 476117

HGVS (amino-acid)	Matching Registered Transcripts
NP_116034.2:p.Asn335Ser	CA5976460 NM_032645.5:c.1004A>G