Allele Registry

Canonical Allele Identifier: PA112931

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000132562

ClinVar Variation:

143055

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Ala488Pro	CA170077 NM_003995.4:c.1462G>C