Canonical Allele Identifier: PA256888
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Arg627Trp
CA256887
NM_002693.3:c.1879C>T