Allele Registry

Canonical Allele Identifier: PA2573075885

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000416364

ClinVar Variation:

375291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Cys771Arg	CA16044042 NM_001378923.1:c.2311T>C