Canonical Allele Identifier: CA414804100
Gene: MT-CO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.9958T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9958T>C , J01415.2:m.9958T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000362079.2:c.752T>C ENSP00000354982.2:p.Phe251Ser
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