Canonical Allele Identifier: PA2828432611
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2940561
ClinVar RCV Id: RCV003799871

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Gly133Ser
CA395866844
NM_001370466.1:c.397G>A