Canonical Allele Identifier: PA2573278379
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1371592
ClinVar RCV Id: RCV002551654
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.His520Arg
CA8051571
NM_022162.3:c.1559A>G