Canonical Allele Identifier: PA2828433142
Gene: NOD2 HGNC NCBI
ClinVar RCV:
RCV000258046
ClinVar Variation:
267317
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Val789Ile
CA10590109
NM_001370466.1:c.2365G>A