Canonical Allele Identifier: PA2829480979
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1299621
ClinVar RCV Id: RCV001730094 RCV001861028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg557His
CA5051777
NM_003995.4:c.1670G>A