Canonical Allele Identifier: PA2828433021
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2950157
ClinVar RCV Id: RCV003807515
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Thr647Ala
CA395870591
NM_001370466.1:c.1939A>G