Allele Registry

Canonical Allele Identifier: PA2829576186

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV001938528

ClinVar Variation:

1417647

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Arg164Gly	CA380333737 NM_005055.5:c.490C>G