Allele Registry

Canonical Allele Identifier: PA2741879156

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV003790429

ClinVar Variation:

2933311

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Ala491Thr	CA192767964 NM_001378923.1:c.1471G>A