Canonical Allele Identifier: CA414797669
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692965
ClinVar RCV Id: RCV000854304
dbSNP Id: rs1603221734
MyVariant Identifiers: chrMT:g.8723G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8723G>A , J01415.2:m.8723G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361899.2:c.197G>A ENSP00000354632.2:p.Arg66Gln
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