Canonical Allele Identifier: PA645494169
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319424
ClinVar RCV Id: RCV000322676 RCV001590949 RCV001782788 RCV002522852
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser47Leu
CA8051207
NM_022162.3:c.140C>T