Canonical Allele Identifier: CA414798284
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 1326901
ClinVar RCV Id: RCV001787286
dbSNP Id: rs1603221825
MyVariant Identifiers: chrMT:g.8821T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8821T>A , J01415.2:m.8821T>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.295T>A ENSP00000354632.2:p.Ser99Thr