Canonical Allele Identifier: CA414795702
Gene: MT-CO2 HGNC NCBI

Linked Data

ClinVar Variation Id: 692829
ClinVar RCV Id: RCV000854157
dbSNP Id: rs1603221351
MyVariant Identifiers: chrMT:g.8252C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8252C>T , J01415.2:m.8252C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361739.1:c.667C>T ENSP00000354876.1:p.Pro223Ser
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