Canonical Allele Identifier: PA2828432662
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 961890
ClinVar RCV Id: RCV002567899

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ser211Gly
CA281261395
NM_001370466.1:c.631A>G