Canonical Allele Identifier: PA2826835569
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_001280486.1:p.His469Leu
CA117025
NM_001293557.2:c.1406A>T