Canonical Allele Identifier: PA102117
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.His932Tyr
CA256891
NM_001126131.2:c.2794C>T