Canonical Allele Identifier: PA916064270
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 808038
ClinVar RCV Id: RCV000996262

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Arg143Lys
CA395866624
NM_022162.3:c.428G>A