Allele Registry

Canonical Allele Identifier: PA645294172

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000416364

ClinVar Variation:

375291

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Cys768Arg	CA16044042 NM_003995.4:c.2302T>C