Canonical Allele Identifier: CA913181325
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 805025
ClinVar RCV Id: RCV000992336
dbSNP Id: rs1603220438
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6353A>G , J01415.2:m.6353A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.450A>G ENSP00000354499.2:p.Leu150=
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