Allele Registry

Canonical Allele Identifier: PA112940

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000132561

ClinVar Variation:

143054

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Arg655Cys	CA170076 NM_003995.4:c.1963C>T