Canonical Allele Identifier: PA316893
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206627
ClinVar RCV Id: RCV000188693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Pro373Leu
CA316892
NM_002693.3:c.1118C>T