Allele Registry

Canonical Allele Identifier: PA2828800311

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV001348167

RCV001358437

ClinVar Variation:

1043981

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Arg263His	CA5051510 NM_001378923.1:c.788G>A