Canonical Allele Identifier: CA913173800
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693880
ClinVar RCV Id: RCV000855287
dbSNP Id: rs1603225265

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15413T>C , J01415.2:m.15413T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.667T>C ENSP00000354554.2:p.Tyr223His