Canonical Allele Identifier: CA414802085
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693072
ClinVar RCV Id: RCV000854418
dbSNP Id: rs1603222028
MyVariant Identifiers: chrMT:g.9067A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9067A>G , J01415.2:m.9067A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361899.2:c.541A>G ENSP00000354632.2:p.Ile181Val
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