Allele Registry

Canonical Allele Identifier: PA112996

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000019362

ClinVar Variation:

17784

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Pro32Thr	CA250692 NM_003995.4:c.94C>A