Canonical Allele Identifier: PA2828432906
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97834
ClinVar RCV Id: RCV000084091 RCV002513872
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Met486Thr
CA150217
NM_001370466.1:c.1457T>C