Allele Registry

Canonical Allele Identifier: PA645500738

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000443235

RCV001833532

RCV001861510

ClinVar Variation:

381703

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Arg91Cys	CA5976769 NM_005055.5:c.271C>T