Canonical Allele Identifier: PA645294178
Gene: NPR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423845
ClinVar RCV Id: RCV000487025
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003986.2:p.Arg848Trp
CA5052002
NM_003995.4:c.2542C>T