Canonical Allele Identifier: PA150341
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97879
ClinVar RCV Id: RCV000328605 RCV001781431 RCV002514488 RCV002262680
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg235Cys
CA150339
NM_022162.3:c.703C>T