Canonical Allele Identifier: PA2828432537
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319424
ClinVar RCV Id: RCV000322676 RCV001590949 RCV001782788 RCV002522852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ser20Leu
CA8051207
NM_001370466.1:c.59C>T