Allele Registry

Canonical Allele Identifier: PA2573075908

Gene: NPR2 HGNC NCBI

ClinVar Allele:

407707

ClinVar RCV:

RCV000480765

RCV000985136

RCV002469165

RCV003766658

ClinVar Variation:

418389

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Arg992Leu	CA16618861 NM_001378923.1:c.2975G>T