Allele Registry

Canonical Allele Identifier: PA2829480948

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV003790429

ClinVar Variation:

2933311

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Ala488Thr	CA192767964 NM_003995.4:c.1462G>A