Canonical Allele Identifier: PA1139715816
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 944231
ClinVar RCV Id: RCV001214587
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg423Gln
CA5051646
NM_003995.4:c.1268G>A