Canonical Allele Identifier: CA414803629
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693215
ClinVar RCV Id: RCV000854568
dbSNP Id: rs1603222471
MyVariant Identifiers: chrMT:g.9751T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9751T>C , J01415.2:m.9751T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.545T>C ENSP00000354982.2:p.Phe182Ser
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