Canonical Allele Identifier: PA1139746104
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 863158
ClinVar RCV Id: RCV002555893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg543Cys
CA8051597
NM_022162.3:c.1627C>T