Canonical Allele Identifier: PA2826835741
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97845
ClinVar RCV Id: RCV000084102 RCV002513877 RCV002505016
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Pro700Leu
CA150247
NM_001293557.2:c.2099C>T