Canonical Allele Identifier: PA2826835280
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319426
ClinVar RCV Id: RCV000330156 RCV001782790 RCV001812838 RCV002521018 RCV002261054 RCV003969902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Asp127Asn
CA8051281
NM_001293557.2:c.379G>A