Canonical Allele Identifier: PA110536
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 4698
ClinVar RCV Id: RCV000416481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.His496Leu
CA117025
NM_022162.3:c.1487A>T