Canonical Allele Identifier: CA913172716
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693811
ClinVar RCV Id: RCV000855207
dbSNP Id: rs1603225024
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15016C>A , J01415.2:m.15016C>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.270C>A ENSP00000354554.2:p.Phe90Leu
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