Canonical Allele Identifier: PA2828432783
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97823
ClinVar RCV Id: RCV000084078 RCV002514469
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Arg364Cys
CA150181
NM_001370466.1:c.1090C>T