Canonical Allele Identifier: PA112996
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 17784
ClinVar RCV Id: RCV000019362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Pro32Thr
CA250692
NM_003995.4:c.94C>A