Allele Registry

Canonical Allele Identifier: PA2573075893

Gene: NPR2 HGNC NCBI

ClinVar RCV:

RCV000132560

ClinVar Variation:

143053

HGVS (amino-acid)	Matching Registered Transcripts
NP_001365852.1:p.Val886Met	CA170074 NM_001378923.1:c.2656G>A