Canonical Allele Identifier: PA2499288903
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1001128
ClinVar RCV Id: RCV002541842

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ser127Leu
CA8051266
NM_022162.3:c.380C>T