Canonical Allele Identifier: PA1139745773
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 961890
ClinVar RCV Id: RCV002567899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser238Gly
CA281261395
NM_022162.3:c.712A>G