Canonical Allele Identifier: PA2499265320
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037301
ClinVar RCV Id: RCV001340432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg218Trp
CA5051480
NM_003995.4:c.652C>T