Allele Registry

Canonical Allele Identifier: PA2829575910

Gene: RAPSN HGNC NCBI

ClinVar RCV:

RCV002579002

ClinVar Variation:

2175150

HGVS (amino-acid)	Matching Registered Transcripts
NP_005046.2:p.Val45Leu	CA221723367 NM_005055.5:c.133G>T CA221723373 NM_005055.5:c.133G>C