Canonical Allele Identifier: PA114783
Gene: ATG16L1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1130
ClinVar RCV Id: RCV000001189 RCV000180346 RCV003982820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060444.3:p.Thr281Ala
CA114782
NM_017974.4:c.841A>G