Allele Registry

Canonical Allele Identifier: PA2741913000

Gene: SSPN HGNC NCBI

ClinVar RCV:

RCV004321224

ClinVar Variation:

2547158

HGVS (amino-acid)	Matching Registered Transcripts
NP_005077.2:p.Arg12Thr	CA384327991 NM_005086.5:c.35G>C