Allele Registry

Canonical Allele Identifier: PA2580211427

Gene: SAP25 HGNC NCBI

ClinVar RCV:

RCV004147604

ClinVar Variation:

2298443

HGVS (amino-acid)	Matching Registered Transcripts
NP_001335609.1:p.Arg224His	CA368522884 NM_001348680.2:c.671G>A