Allele Registry

Canonical Allele Identifier: PA113011

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000019363

ClinVar Variation:

17785

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Trp115Gly	CA250693 NM_003995.4:c.343T>G