Canonical Allele Identifier: CA10581314
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 235451
ClinVar RCV Id: RCV000224303
dbSNP Id: rs878853038
MyVariant Identifiers: chrMT:g.8619C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8619C>T , J01415.2:m.8619C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.93C>T ENSP00000354632.2:p.Ile31=