Canonical Allele Identifier: PA916048489
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531606
ClinVar RCV Id: RCV002261144 RCV002529867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ala78Val
CA8051250
NM_001370466.1:c.233C>T