Canonical Allele Identifier: PA1139746010
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 947025
ClinVar RCV Id: RCV001218005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Val487Asp
CA395868963
NM_022162.3:c.1460T>A