Allele Registry

Canonical Allele Identifier: PA645413948

Gene: PSAP HGNC NCBI

ClinVar RCV:

RCV000484673

RCV001084808

RCV001272680

RCV001335064

RCV003902722

ClinVar Variation:

418428

HGVS (amino-acid)	Matching Registered Transcripts
NP_002769.1:p.Leu137Val	CA5547774 NM_002778.4:c.409C>G