Canonical Allele Identifier: PA113011
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17785
ClinVar RCV Id: RCV000019363
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Trp115Gly
CA250693
NM_003995.4:c.343T>G