Canonical Allele Identifier: CA414804118
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693253
ClinVar RCV Id: RCV000854609
dbSNP Id: rs200809063
MyVariant Identifiers: chrMT:g.9966G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9966G>C , J01415.2:m.9966G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.760G>C ENSP00000354982.2:p.Val254Leu
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