Canonical Allele Identifier: PA316597
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206470

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Ala1033Val
CA316596
NM_002693.3:c.3098C>T