Canonical Allele Identifier: PA102141
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13497

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.Leu304Arg
CA256883
NM_001126131.2:c.911T>G