Canonical Allele Identifier: PA891852213
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 583173
ClinVar RCV Id: RCV000707442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Pro438His
CA373371237
NM_003995.4:c.1313C>A