Canonical Allele Identifier: PA2828432671
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531608
ClinVar RCV Id: RCV001811130 RCV002529869
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Glu222Gly
CA8051389
NM_001370466.1:c.665A>G