Allele Registry

Canonical Allele Identifier: PA2829578422

Gene: SSPN HGNC NCBI

ClinVar RCV:

RCV004305677

ClinVar Variation:

2530905

HGVS (amino-acid)	Matching Registered Transcripts
NP_005077.2:p.Val135Phe	CA6487943 NM_005086.5:c.403G>T