Canonical Allele Identifier: PA658668390
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 462698
ClinVar RCV Id: RCV002261099 RCV002528346
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gly680Arg
CA8051678
NM_022162.3:c.2038G>A
CA395870655
NM_022162.3:c.2038G>C