Allele Registry

Canonical Allele Identifier: PA2499265322

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV001348167

RCV001358437

ClinVar Variation:

1043981

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Arg263His	CA5051510 NM_003995.4:c.788G>A