Allele Registry

Canonical Allele Identifier: PA2828432892

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000416481

ClinVar Variation:

4698

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.His469Leu	CA117025 NM_001370466.1:c.1406A>T