Canonical Allele Identifier: PA2828432681
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1022922
ClinVar RCV Id: RCV002543846
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Met238Leu
CA395867578
NM_001370466.1:c.712A>C
CA395867579
NM_001370466.1:c.712A>T