Canonical Allele Identifier: PA150261
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97849
ClinVar RCV Id: RCV000084106 RCV001781419 RCV002513878
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg791Trp
CA150259
NM_022162.3:c.2371C>T