Canonical Allele Identifier: PA316816
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206586

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Arg288Cys
CA316815
NM_002693.3:c.862C>T