Canonical Allele Identifier: PA916064576
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 644507
ClinVar RCV Id: RCV002537091 RCV002537090
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Glu748Lys
CA8051735
NM_022162.3:c.2242G>A