Canonical Allele Identifier: PA2828800284
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 375293
ClinVar RCV Id: RCV000416349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Val187Asp
CA16044040
NM_001378923.1:c.560T>A