Canonical Allele Identifier: PA2828800236
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 366777
ClinVar RCV Id: RCV000333349

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001365852.1:p.Glu33Ala
CA10627306
NM_001378923.1:c.98A>C