Allele Registry

Canonical Allele Identifier: PA916071644

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000548221

RCV001103570

RCV001103571

ClinVar Variation:

476122

HGVS (amino-acid)	Matching Registered Transcripts
NP_116034.2:p.Val214Met	CA5976688 NM_032645.5:c.640G>A