Canonical Allele Identifier: CA414804099
Gene: MT-CO3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.9957T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9957T>G , J01415.2:m.9957T>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000362079.2:c.751T>G ENSP00000354982.2:p.Phe251Val
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