Allele Registry

Canonical Allele Identifier: PA2826156990

Gene: ATG16L1 HGNC NCBI

ClinVar RCV:

RCV000001189

RCV000180346

RCV003982820

ClinVar Variation:

1130

HGVS (amino-acid)	Matching Registered Transcripts
NP_001177195.1:p.Thr216Ala	CA114782 NM_001190266.2:c.646A>G