Allele Registry

Canonical Allele Identifier: PA645294148

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000490251

ClinVar Variation:

427217

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Pro47Leu	CA373361725 NM_003995.4:c.140C>T