Canonical Allele Identifier: CA913174621
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693936
ClinVar RCV Id: RCV000855354
dbSNP Id: rs1556424649
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15708G>C , J01415.2:m.15708G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.962G>C ENSP00000354554.2:p.Ser321Thr
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