Canonical Allele Identifier: PA2828432980
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4700
ClinVar RCV Id: RCV000328692 RCV001280996 RCV001781188 RCV002512787 RCV003421904 RCV003224090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ala585Thr
CA117029
NM_001370466.1:c.1753G>A