Canonical Allele Identifier: CA414792009
Gene: MT-CO1 HGNC NCBI

Linked Data

ClinVar Variation Id: 692718
ClinVar RCV Id: RCV000854043
dbSNP Id: rs1603220839
MyVariant Identifiers: chrMT:g.7233C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7233C>T , J01415.2:m.7233C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361624.2:c.1330C>T ENSP00000354499.2:p.Pro444Ser