Canonical Allele Identifier: CA913174250
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693908
ClinVar RCV Id: RCV000855324
dbSNP Id: rs1603225356
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15575G>A , J01415.2:m.15575G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.829G>A ENSP00000354554.2:p.Ala277Thr
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