Canonical Allele Identifier: CA414798670
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 918021
ClinVar RCV Id: RCV001175268
dbSNP Id: rs2068712730
MyVariant Identifiers: chrMT:g.8878C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8878C>T , J01415.2:m.8878C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.352C>T ENSP00000354632.2:p.Arg118Cys