Canonical Allele Identifier: PA316891
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Asn354Asp
CA316890
NM_002693.3:c.1060A>G