Canonical Allele Identifier: PA2826835611
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319448
ClinVar RCV Id: RCV000355684 RCV001782812 RCV001812846 RCV002522859
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Pro518Leu
CA8051599
NM_001293557.2:c.1553C>T