Canonical Allele Identifier: PA150174
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97820
ClinVar RCV Id: RCV000084074 RCV002514468
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ile363Phe
CA150172
NM_022162.3:c.1087A>T