Canonical Allele Identifier: PA2826835291
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 858593
ClinVar RCV Id: RCV001311447 RCV002555831
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280486.1:p.Glu139Asp
CA8051291
NM_001293557.2:c.417A>T
CA395866928
NM_001293557.2:c.417A>C