Canonical Allele Identifier: PA2741976200
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2950157
ClinVar RCV Id: RCV003807515
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Thr674Ala
CA395870591
NM_022162.3:c.2020A>G