Canonical Allele Identifier: PA110492
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4696
ClinVar RCV Id: RCV000004960 RCV001509512 RCV002512785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg334Trp
CA117022
NM_022162.3:c.1000C>T