Canonical Allele Identifier: PA2826835570
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 565494
ClinVar RCV Id: RCV002531432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Glu471Asp
CA395869044
NM_001293557.2:c.1413A>C
CA395869045
NM_001293557.2:c.1413A>T