Canonical Allele Identifier: CA337097902
Gene: MT-ATP8 HGNC NCBI

Linked Data

dbSNP Id: rs369661971
MyVariant Identifiers: chrMT:g.8485G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8485G>A , J01415.2:m.8485G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.120G>A ENSP00000355265.1:p.Lys40=
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