Canonical Allele Identifier: PA102275
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 13507

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.Trp748Ser
CA123150
NM_001126131.2:c.2243G>C