Allele Registry

Canonical Allele Identifier: PA645294151

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000416349

ClinVar Variation:

375293

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Val187Asp	CA16044040 NM_003995.4:c.560T>A