Canonical Allele Identifier: PA2828432538
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1500548
ClinVar RCV Id: RCV002657655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Gly21Ala
CA281250013
NM_001370466.1:c.62G>C