Canonical Allele Identifier: PA2499256208
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_001365852.1:p.Arg560His
CA5051777
NM_001378923.1:c.1679G>A