Canonical Allele Identifier: PA645294187
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 418389
ClinVar RCV Id: RCV000480765 RCV000985136 RCV002469165 RCV003766658
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg989Leu
CA16618861
NM_003995.4:c.2966G>T