Allele Registry

Canonical Allele Identifier: PA645294156

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000414841

ClinVar Variation:

373988

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Glu260Val	CA16043443 NM_003995.4:c.779A>T