Canonical Allele Identifier: CA414802320
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 441146
ClinVar RCV Id: RCV000509437 RCV000854461
dbSNP Id: rs1556423625
MyVariant Identifiers: chrMT:g.9157G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9157G>A , J01415.2:m.9157G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.631G>A ENSP00000354632.2:p.Ala211Thr
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