Canonical Allele Identifier: PA1139742999
Gene: NOD2 HGNC NCBI

Linked Data

ClinVar Variation Id: 859623
ClinVar RCV Id: RCV003103920

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001357395.1:p.His99Asp
CA8051264
NM_001370466.1:c.295C>G