Canonical Allele Identifier: PA645294153
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 366780
ClinVar RCV Id: RCV000315791 RCV000946345
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Ile217Phe
CA5051478
NM_003995.4:c.649A>T