Canonical Allele Identifier: PA2826835581
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2936815
ClinVar RCV Id: RCV003799053

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Thr482Ser
CA395869109
NM_001293557.2:c.1444A>T
CA395869110
NM_001293557.2:c.1445C>G