Allele Registry

Canonical Allele Identifier: PA2741913002

Gene: SSPN HGNC NCBI

ClinVar RCV:

RCV004311755

ClinVar Variation:

2540384

HGVS (amino-acid)	Matching Registered Transcripts
NP_005077.2:p.Val67Met	CA6487871 NM_005086.5:c.199G>A