Canonical Allele Identifier: PA2573277992
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1500548
ClinVar RCV Id: RCV002657655

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Gly48Ala
CA281250013
NM_022162.3:c.143G>C