Allele Registry

Canonical Allele Identifier: PA2825403671

Gene: PSAP HGNC NCBI

ClinVar RCV:

RCV001921495

RCV002291509

RCV003339831

ClinVar Variation:

1424237

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035931.1:p.Val294Gly	CA5547587 NM_001042466.3:c.881T>G