Allele Registry

Canonical Allele Identifier: PA2825403404

Gene: PSAP HGNC NCBI

ClinVar RCV:

RCV000512836

RCV001087790

RCV001834647

RCV003960205

ClinVar Variation:

444224

HGVS (amino-acid)	Matching Registered Transcripts
NP_001035931.1:p.Leu4Val	CA5547944 NM_001042466.3:c.10C>G