Allele Registry

Canonical Allele Identifier: PA658659892

Gene: PSAP HGNC NCBI

ClinVar Allele:

438867

ClinVar RCV:

RCV000514444

RCV001081218

RCV001272678

RCV003962415

ClinVar Variation:

445595

HGVS (amino-acid)	Matching Registered Transcripts
NP_002769.1:p.Ile208Ser	CA5547714 NM_002778.4:c.623T>G