Allele Registry

Canonical Allele Identifier: PA2741913003

Gene: SSPN HGNC NCBI

ClinVar RCV:

RCV004312625

ClinVar Variation:

2534645

HGVS (amino-acid)	Matching Registered Transcripts
NP_005077.2:p.Ser76Gly	CA384328380 NM_005086.5:c.226A>G