Canonical Allele Identifier: PA264782
Gene: DPAGT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65469
ClinVar RCV Id: RCV000055659 RCV001291448
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373.2:p.Ala114Gly
CA264781
NM_001382.4:c.341C>G