Canonical Allele Identifier: CA913180885
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 918025
ClinVar RCV Id: RCV001175273
dbSNP Id: rs879181854
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8946A>T , J01415.2:m.8946A>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361899.2:c.420A>T ENSP00000354632.2:p.Ile140=
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