Allele Registry

Canonical Allele Identifier: PA2828432790

Gene: NOD2 HGNC NCBI

ClinVar Allele:

530342

ClinVar RCV:

RCV001118317

RCV001784213

RCV001811129

RCV002263872

RCV002528894

RCV003905719

ClinVar Variation:

531599

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Pro370Leu	CA8051488 NM_001370466.1:c.1109C>T