Canonical Allele Identifier: PA645494174
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_071445.1:p.Asp154Asn
CA8051281
NM_022162.3:c.460G>A