Canonical Allele Identifier: CA414799046
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693028
ClinVar RCV Id: RCV000854369
dbSNP Id: rs1603221920
MyVariant Identifiers: chrMT:g.8936T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8936T>C , J01415.2:m.8936T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.410T>C ENSP00000354632.2:p.Leu137Pro