Allele Registry

Canonical Allele Identifier: PA2826271310

Gene: NPR3 HGNC NCBI

ClinVar RCV:

RCV001423797

ClinVar Variation:

1101009

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191305.1:p.Gly261Ser	CA3222669 NM_001204376.2:c.781G>A