Allele Registry

Canonical Allele Identifier: PA2828800312

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000190430

RCV002514080

ClinVar Variation:

208358

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Arg263Pro	CA204430 NM_001378923.1:c.788G>C