Canonical Allele Identifier: CA913172710
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693810
ClinVar RCV Id: RCV000855206
dbSNP Id: rs1603225022

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15014T>C , J01415.2:m.15014T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.268T>C ENSP00000354554.2:p.Phe90Leu