Canonical Allele Identifier: PA2828800293
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_001365852.1:p.Arg218Trp
CA5051480
NM_001378923.1:c.652C>T