Allele Registry

Canonical Allele Identifier: PA099835

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008521

RCV000704275

RCV000992743

RCV001275253

RCV002476946

RCV003460442

ClinVar Variation:

8055

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Val45Met	CA119257 NM_005055.5:c.133G>A