Canonical Allele Identifier: PA658808546
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531606
ClinVar RCV Id: RCV002261144 RCV002529867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala105Val
CA8051250
NM_022162.3:c.314C>T