Canonical Allele Identifier: CA414802416
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693123
ClinVar RCV Id: RCV000854474
dbSNP Id: rs1603222169
MyVariant Identifiers: chrMT:g.9202A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9202A>G , J01415.2:m.9202A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.676A>G ENSP00000354632.2:p.Thr226Ala
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