Allele Registry

Canonical Allele Identifier: PA2828800292

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000315791

RCV000946345

ClinVar Variation:

366780

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Ile217Phe	CA5051478 NM_001378923.1:c.649A>T