Canonical Allele Identifier: PA102149
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 426681
ClinVar RCV Id: RCV000489004 RCV000758421 RCV001526408 RCV003985792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001119603.1:p.Lys1191Asn
CA10602282
NM_001126131.2:c.3573G>T
CA393747470
NM_001126131.2:c.3573G>C