Allele Registry

Canonical Allele Identifier: PA2828432979

Gene: NOD2 HGNC NCBI

ClinVar RCV:

RCV000293577

RCV000385541

RCV002521035

RCV003972363

ClinVar Variation:

319452

HGVS (amino-acid)	Matching Registered Transcripts
NP_001357395.1:p.Ala585Ser	CA8051634 NM_001370466.1:c.1753G>T