Canonical Allele Identifier: PA2826835460
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97823
ClinVar RCV Id: RCV000084078 RCV002514469
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Arg364Cys
CA150181
NM_001293557.2:c.1090C>T