Canonical Allele Identifier: PA112924
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1434966
ClinVar RCV Id: RCV001984760
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Ala409Thr
CA373370903
NM_003995.4:c.1225G>A