Canonical Allele Identifier: PA2828432898
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948891
ClinVar RCV Id: RCV003801617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Gly477Arg
CA395869079
NM_001370466.1:c.1429G>A
CA395869080
NM_001370466.1:c.1429G>C