Canonical Allele Identifier: PA1139717990
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 946586
ClinVar RCV Id: RCV001217482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Ala341Asp
CA1139664124
NM_002693.3:c.1022_1023delinsAT