Allele Registry

Canonical Allele Identifier: PA2826271324

Gene: NPR3 HGNC NCBI

ClinVar RCV:

RCV001641090

ClinVar Variation:

1240702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191305.1:p.Asn305Asp	CA3222712 NM_001204376.2:c.913A>G