Allele Registry

Canonical Allele Identifier: PA112950

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV001733607

RCV002032734

ClinVar Variation:

1301658

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Arg776Trp	CA373379257 NM_003995.4:c.2326C>T