Allele Registry

Canonical Allele Identifier: PA2573075880

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000132561

ClinVar Variation:

143054

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Arg658Cys	CA170076 NM_001378923.1:c.1972C>T