Allele Registry

Canonical Allele Identifier: PA2825367244

Gene: NPNT HGNC NCBI

ClinVar RCV:

RCV004075220

ClinVar Variation:

2211604

HGVS (amino-acid)	Matching Registered Transcripts
NP_001028219.1:p.Gly516Val	CA3034542 NM_001033047.3:c.1547G>T