Canonical Allele Identifier: PA2826835218
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 267320
ClinVar RCV Id: RCV000258045 RCV002519022
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Leu54Val
CA8051231
NM_001293557.2:c.160C>G