Canonical Allele Identifier: PA2826835563
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1184615
ClinVar RCV Id: RCV001542792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Met464Leu
CA395868988
NM_001293557.2:c.1390A>C
CA395868990
NM_001293557.2:c.1390A>T