Canonical Allele Identifier: CA414803649
Gene: MT-CO3 HGNC NCBI

Linked Data

ClinVar Variation Id: 693222
ClinVar RCV Id: RCV000854575
dbSNP Id: rs1603222483
MyVariant Identifiers: chrMT:g.9759C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9759C>T , J01415.2:m.9759C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000362079.2:c.553C>T ENSP00000354982.2:p.Pro185Ser
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