Allele Registry

Canonical Allele Identifier: PA2499242096

Gene: NPR3 HGNC NCBI

ClinVar RCV:

RCV001641090

ClinVar Variation:

1240702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191304.1:p.Asn522Asp	CA3222712 NM_001204375.2:c.1564A>G