Canonical Allele Identifier: PA658659101
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 450409
ClinVar RCV Id: RCV000519551
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg58Pro
CA192760671
NM_003995.4:c.173G>C