Allele Registry

Canonical Allele Identifier: PA2829382135

Gene: PSAP HGNC NCBI

ClinVar RCV:

RCV001921495

RCV002291509

RCV003339831

ClinVar Variation:

1424237

HGVS (amino-acid)	Matching Registered Transcripts
NP_002769.1:p.Val292Gly	CA5547587 NM_002778.4:c.875T>G