Canonical Allele Identifier: PA150183
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_071445.1:p.Arg391Cys
CA150181
NM_022162.3:c.1171C>T