Canonical Allele Identifier: CA337098241
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693109
ClinVar RCV Id: RCV000854457
dbSNP Id: rs200660596
MyVariant Identifiers: chrMT:g.9142G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9142G>A , J01415.2:m.9142G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.616G>A ENSP00000354632.2:p.Val206Ile
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