Canonical Allele Identifier: PA2828432929
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1124621
ClinVar RCV Id: RCV002557560
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg514Gln
CA8051595
NM_001370466.1:c.1541G>A