Allele Registry

Canonical Allele Identifier: PA2828149595

Gene: NPR3 HGNC NCBI

ClinVar RCV:

RCV001641090

ClinVar Variation:

1240702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001351389.1:p.Asn265Asp	CA3222712 NM_001364460.2:c.793A>G