Allele Registry

Canonical Allele Identifier: PA095995

Gene: PSPH HGNC NCBI

ClinVar RCV:

RCV000014593

ClinVar Variation:

13623

HGVS (amino-acid)	Matching Registered Transcripts
NP_004568.2:p.Asp32Asn	CA123295 NM_004577.4:c.94G>A