Canonical Allele Identifier: PA150279
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97855
ClinVar RCV Id: RCV000381377 RCV001781423 RCV002260983 RCV003736574 RCV002513882
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala849Val
CA150277
NM_022162.3:c.2546C>T