Canonical Allele Identifier: PA2825620629
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206581

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.Gln226His
CA316806
NM_001126131.2:c.678G>C
CA393767261
NM_001126131.2:c.678G>T