Canonical Allele Identifier: CA337098175
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693071
ClinVar RCV Id: RCV000854417
dbSNP Id: rs386420013
MyVariant Identifiers: chrMT:g.9064G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9064G>A , J01415.2:m.9064G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.538G>A ENSP00000354632.2:p.Ala180Thr