Canonical Allele Identifier: CA414793205
Gene: MT-CO2 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.7662A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7662A>T , J01415.2:m.7662A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.77A>T ENSP00000354876.1:p.His26Leu
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