Canonical Allele Identifier: CA913172606
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693800
ClinVar RCV Id: RCV000855195
dbSNP Id: rs1603224997

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14976G>A , J01415.2:m.14976G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.230G>A ENSP00000354554.2:p.Ter77=