Canonical Allele Identifier: PA2580282508
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2160347
ClinVar RCV Id: RCV003075903
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Tyr254His
CA192762944
NM_003995.4:c.760T>C