Canonical Allele Identifier: PA2828433231
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 994371
ClinVar RCV Id: RCV001810603
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ser901Asn
CA8051966
NM_001370466.1:c.2702G>A