Allele Registry

Canonical Allele Identifier: PA2825367246

Gene: NPNT HGNC NCBI

ClinVar RCV:

RCV004075221

ClinVar Variation:

2211605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028219.1:p.Arg528Gln	CA3034550 NM_001033047.3:c.1583G>A