Allele Registry

Canonical Allele Identifier: PA2573075907

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000416371

ClinVar Variation:

375294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Asp985Asn	CA16044043 NM_001378923.1:c.2953G>A