Allele Registry

Canonical Allele Identifier: PA2573075872

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000132562

ClinVar Variation:

143055

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Ala491Pro	CA170077 NM_001378923.1:c.1471G>C