Canonical Allele Identifier: PA645494242
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319452

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala612Ser
CA8051634
NM_022162.3:c.1834G>T