Canonical Allele Identifier: CA913173203
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 2664158
ClinVar RCV Id: RCV003445293
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15192T>G , J01415.2:m.15192T>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.446T>G ENSP00000354554.2:p.Leu149Ter
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