Canonical Allele Identifier: PA2828433098
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319462
ClinVar RCV Id: RCV000341511 RCV000513725 RCV001782824 RCV002263017 RCV002056495 RCV002521040 RCV003920348
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ala728Val
CA8051743
NM_001370466.1:c.2183C>T