Canonical Allele Identifier: PA2828432648
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 493181

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Ala184Ser
CA395867222
NM_001370466.1:c.550G>T