Canonical Allele Identifier: CA414797539
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692956
ClinVar RCV Id: RCV000854294
dbSNP Id: rs1603221713
MyVariant Identifiers: chrMT:g.8702C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8702C>T , J01415.2:m.8702C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.176C>T ENSP00000354632.2:p.Thr59Ile