Canonical Allele Identifier: PA2826835801
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_001280486.1:p.Arg764Trp
CA150259
NM_001293557.2:c.2290C>T