Allele Registry

Canonical Allele Identifier: PA2828101099

Gene: NPR3 HGNC NCBI

ClinVar RCV:

RCV001641090

ClinVar Variation:

1240702

HGVS (amino-acid)	Matching Registered Transcripts
NP_001350581.1:p.Asn306Asp	CA3222712 NM_001363652.2:c.916A>G