Allele Registry

Canonical Allele Identifier: PA099756

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV000008525

ClinVar Variation:

8059

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Ala189Val	CA119260 NM_005055.5:c.566C>T