Allele Registry

Canonical Allele Identifier: PA2828800259

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000190431

RCV001263517

RCV001781561

RCV001857670

ClinVar Variation:

208359

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Arg110Cys	CA204432 NM_001378923.1:c.328C>T