Canonical Allele Identifier: CA414784781
Gene: MT-CO1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.6561T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.6561T>G , J01415.2:m.6561T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.658T>G ENSP00000354499.2:p.Phe220Val
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