Canonical Allele Identifier: PA2828432698
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319440
ClinVar RCV Id: RCV001121730 RCV001726112 RCV001702425 RCV001782804 RCV002263013 RCV002521029 RCV003972362
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Asn262Ser
CA8051413
NM_001370466.1:c.785A>G