Canonical Allele Identifier: PA645494183
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319438
ClinVar RCV Id: RCV000287407 RCV001782802 RCV002521026 RCV002521027 RCV003114482
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071445.1:p.Leu281Phe
CA8051409
NM_022162.3:c.841C>T