Allele Registry

Canonical Allele Identifier: PA2826141787

Gene: NPNT HGNC NCBI

ClinVar RCV:

RCV004075221

ClinVar Variation:

2211605

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171619.1:p.Arg545Gln	CA3034550 NM_001184690.2:c.1634G>A