Canonical Allele Identifier: PA2826835277
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2937622
ClinVar RCV Id: RCV003794252

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Met125Ile
CA395866753
NM_001293557.2:c.375G>A
CA395866755
NM_001293557.2:c.375G>C
CA395866756
NM_001293557.2:c.375G>T