Allele Registry

Canonical Allele Identifier: PA2828800263

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000019363

ClinVar Variation:

17785

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Trp115Gly	CA250693 NM_001378923.1:c.343T>G