Canonical Allele Identifier: PA2828432696
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319439
ClinVar RCV Id: RCV000344671 RCV001782803 RCV002521028
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.His260Tyr
CA8051412
NM_001370466.1:c.778C>T