Allele Registry

Canonical Allele Identifier: PA2825403104

Gene: PSAP HGNC NCBI

ClinVar Allele:

322776

ClinVar RCV:

RCV000272506

RCV000274090

RCV000327586

RCV000386828

RCV002522167

RCV004021479

ClinVar Variation:

300533

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035930.1:p.Pro56Arg	CA5547881 NM_001042465.3:c.167C>G