Canonical Allele Identifier: PA1139745669
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_071445.1:p.Glu166Asp
CA8051291
NM_022162.3:c.498A>T
CA395866928
NM_022162.3:c.498A>C