Allele Registry

Canonical Allele Identifier: PA915998493

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000985135

RCV001805952

ClinVar Variation:

800932

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Arg989Gln	CA5052162 NM_003995.4:c.2966G>A