Canonical Allele Identifier: PA2828432888
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2929517
ClinVar RCV Id: RCV003784683
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ser466Phe
CA395869008
NM_001370466.1:c.1397C>T