Canonical Allele Identifier: CA414796838
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692916
ClinVar RCV Id: RCV000854251
dbSNP Id: rs1603221612
MyVariant Identifiers: chrMT:g.8593A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8593A>G , J01415.2:m.8593A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361899.2:c.67A>G ENSP00000354632.2:p.Ile23Val
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