Canonical Allele Identifier: PA2828432860
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4695
ClinVar RCV Id: RCV000004959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Leu442Phe
CA117020
NM_001370466.1:c.1324C>T