Canonical Allele Identifier: CA913177531
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 994646
ClinVar RCV Id: RCV001288247
dbSNP Id: rs2068704310
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7606A>G , J01415.2:m.7606A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361739.1:c.21A>G ENSP00000354876.1:p.Val7=
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