Canonical Allele Identifier: PA2828432693
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319438
ClinVar RCV Id: RCV000287407 RCV001782802 RCV002521026 RCV002521027 RCV003114482
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Leu254Phe
CA8051409
NM_001370466.1:c.760C>T