Canonical Allele Identifier: CA414802234
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693096
ClinVar RCV Id: RCV000854444
dbSNP Id: rs1603222087
MyVariant Identifiers: chrMT:g.9110T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9110T>C , J01415.2:m.9110T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.584T>C ENSP00000354632.2:p.Ile195Thr