Allele Registry

Canonical Allele Identifier: PA099813

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008518

RCV000178899

RCV001255415

RCV001336781

RCV001731282

RCV002512911

RCV003460441

ClinVar Variation:

8052

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Leu283Pro	CA119255 NM_005055.5:c.848T>C