Canonical Allele Identifier: CA913190831
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 590891
ClinVar RCV Id: RCV000768656
dbSNP Id: rs1569484300
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9431_9432insA , J01415.2:m.9431_9432insA GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.225_226insA ENSP00000354982.2:p.Gln76ThrfsTer?
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