Canonical Allele Identifier: PA316851
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 206604

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002684.1:p.Asn630Ser
CA316850
NM_002693.3:c.1889A>G