Allele Registry

Canonical Allele Identifier: PA099801

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008513

RCV001851738

RCV003460439

ClinVar Variation:

8047

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Leu14Pro	CA119252 NM_005055.5:c.41T>C