Allele Registry

Canonical Allele Identifier: PA2828436356

Gene: PSPH HGNC NCBI

ClinVar RCV:

RCV000014593

ClinVar Variation:

13623

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357450.1:p.Asp32Asn	CA123295 NM_001370521.1:c.94G>A