Canonical Allele Identifier: PA2829481061
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2506595
ClinVar RCV Id: RCV003236964
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Phe789Ser
CA373379447
NM_003995.4:c.2366T>C