Canonical Allele Identifier: PA658808560
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 531607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser238Cys
CA395867405
NM_022162.3:c.712A>T