Canonical Allele Identifier: PA150338
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97878

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Trp157Arg
CA150336
NM_022162.3:c.469T>C
CA395866805
NM_022162.3:c.469T>A