Canonical Allele Identifier: PA2573278112
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1431029
ClinVar RCV Id: RCV002560705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Ala224Val
CA8051371
NM_022162.3:c.671C>T