Canonical Allele Identifier: CA913174198
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693906
ClinVar RCV Id: RCV000855322
dbSNP Id: rs1603225350
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15557G>A , J01415.2:m.15557G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.811G>A ENSP00000354554.2:p.Glu271Lys
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