Canonical Allele Identifier: PA2573232741
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1427915
ClinVar RCV Id: RCV001964731
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Glu288Ala
CA5051532
NM_003995.4:c.863A>C