Canonical Allele Identifier: CA337097991
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692955
ClinVar RCV Id: RCV000854293
dbSNP Id: rs2000975
MyVariant Identifiers: chrMT:g.8701A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8701A>G , J01415.2:m.8701A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361899.2:c.175A>G ENSP00000354632.2:p.Thr59Ala