Allele Registry

Canonical Allele Identifier: PA2825217327

Gene: NPR3 HGNC NCBI

ClinVar RCV:

RCV001641090

ClinVar Variation:

1240702

HGVS (amino-acid)	Matching Registered Transcripts
NP_000899.1:p.Asn521Asp	CA3222712 NM_000908.4:c.1561A>G