Canonical Allele Identifier: PA2573232791
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1486654
ClinVar RCV Id: RCV002003758
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Ala408Val
CA373370901
NM_003995.4:c.1223C>T