Canonical Allele Identifier: PA2828433027
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_001357395.1:p.Gly653Arg
CA8051678
NM_001370466.1:c.1957G>A
CA395870655
NM_001370466.1:c.1957G>C