Canonical Allele Identifier: PA2825620830
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206627
ClinVar RCV Id: RCV000188693

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.Pro373Leu
CA316892
NM_001126131.2:c.1118C>T