Canonical Allele Identifier: PA645494220
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319444
ClinVar RCV Id: RCV000379610 RCV000700656 RCV001782808 RCV002521032 RCV003401335
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg439His
CA8051519
NM_022162.3:c.1316G>A