Canonical Allele Identifier: CA414797002
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692930
ClinVar RCV Id: RCV000854266
dbSNP Id: rs1603221645
MyVariant Identifiers: chrMT:g.8623A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8623A>T , J01415.2:m.8623A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.97A>T ENSP00000354632.2:p.Thr33Ser
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