Canonical Allele Identifier: PA658808673
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531609
ClinVar RCV Id: RCV001120441 RCV001784214 RCV002261145 RCV002529870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala976Thr
CA8052024
NM_022162.3:c.2926G>A