Canonical Allele Identifier: PA2828433074
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 267319
ClinVar RCV Id: RCV000258056
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Val706Leu
CA10590111
NM_001370466.1:c.2116G>T
CA395871303
NM_001370466.1:c.2116G>C