Canonical Allele Identifier: PA1139745923
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 853895
ClinVar RCV Id: RCV002554411

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg393Cys
CA8051484
NM_022162.3:c.1177C>T