Allele Registry

Canonical Allele Identifier: PA2829576236

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV001906986

RCV003130594

ClinVar Variation:

1406773

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Arg217His	CA5976686 NM_005055.5:c.650G>A