Allele Registry

Canonical Allele Identifier: PA2828436456

Gene: PSPH HGNC NCBI

ClinVar RCV:

RCV000014593

ClinVar Variation:

13623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357451.1:p.Asp32Asn	CA123295 NM_001370522.1:c.94G>A