Canonical Allele Identifier: CA10581289
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 235370
ClinVar RCV Id: RCV000224874 RCV000854329 RCV003319189
dbSNP Id: rs878853020
MyVariant Identifiers: chrMT:g.8803A>T (hg38)
ERepo: CA10581289/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8803A>T , J01415.2:m.8803A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.277A>T ENSP00000354632.2:p.Thr93Ser
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