Canonical Allele Identifier: CA337098084
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693004
ClinVar RCV Id: RCV000854344
dbSNP Id: rs2001031
MyVariant Identifiers: chrMT:g.8860A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8860A>G , J01415.2:m.8860A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.334A>G ENSP00000354632.2:p.Thr112Ala