Allele Registry

Canonical Allele Identifier: PA916071535

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008521

RCV000704275

RCV000992743

RCV001275253

RCV002476946

RCV003460442

ClinVar Variation:

8055

HGVS (amino-acid)	Matching Registered Transcripts
NP_116034.2:p.Val45Met	CA119257 NM_032645.5:c.133G>A