Canonical Allele Identifier: PA2828433209
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 319471

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.Gln875Lys
CA8051929
NM_001370466.1:c.2623C>A