ClinGen Allele Registry
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Canonical Allele Identifier:
CA414795310
Gene: MT-CO2
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chrMT:g.8165G>A (hg38)
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Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.8165G>A , J01415.2:m.8165G>A
GRCh38
Transcript Alleles
HGVS
Amino-acid Change
ENST00000361739.1:c.580G>A
ENSP00000354876.1:p.Gly194Ser
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