Canonical Allele Identifier: PA316755
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Arg1096Gly
CA316754
NM_002693.3:c.3286C>G