Canonical Allele Identifier: PA2741976054
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2940073
ClinVar RCV Id: RCV003797431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Trp260Cys
CA281261485
NM_022162.3:c.780G>C
CA395867552
NM_022162.3:c.780G>T