Canonical Allele Identifier: PA261217
Gene: DPAGT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39773
ClinVar RCV Id: RCV000032992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373.2:p.Ile69Asn
CA261216
NM_001382.4:c.206T>A