Allele Registry

Canonical Allele Identifier: PA2573075909

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000985135

RCV001805952

ClinVar Variation:

800932

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Arg992Gln	CA5052162 NM_001378923.1:c.2975G>A