Canonical Allele Identifier: CA10581353
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 235548
ClinVar RCV Id: RCV000224265
dbSNP Id: rs878853064
MyVariant Identifiers: chrMT:g.6554C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6554C>T , J01415.2:m.6554C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.651C>T ENSP00000354499.2:p.Thr217=
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