Allele Registry

Canonical Allele Identifier: PA645294160

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000489591

ClinVar Variation:

427026

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Gly378Arg	CA373370518 NM_003995.4:c.1132G>A CA373370520 NM_003995.4:c.1132G>C