Canonical Allele Identifier: CA913174956
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693961
ClinVar RCV Id: RCV000855383
dbSNP Id: rs1603225527
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15828C>T , J01415.2:m.15828C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1082C>T ENSP00000354554.2:p.Thr361Ile
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