Allele Registry

Canonical Allele Identifier: PA275257

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000178236

RCV001313406

RCV003462285

ClinVar Variation:

197248

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Ala246Val	CA275256 NM_005055.5:c.737C>T