Allele Registry

Canonical Allele Identifier: PA2580160460

Gene: NPNT HGNC NCBI

ClinVar RCV:

RCV004075221

ClinVar Variation:

2211605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171620.1:p.Arg558Gln	CA3034550 NM_001184691.2:c.1673G>A