Canonical Allele Identifier: PA1139715527
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 931161
ClinVar RCV Id: RCV001197478 RCV001253507 RCV001859192
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg165His
CA5051456
NM_003995.4:c.494G>A