Allele Registry

Canonical Allele Identifier: PA170075

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000132560

ClinVar Variation:

143053

HGVS (amino-acid)	Matching Registered Transcripts
NP_003986.2:p.Val883Met	CA170074 NM_003995.4:c.2647G>A