Canonical Allele Identifier: CA10581408
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 235707
ClinVar RCV Id: RCV000224200
dbSNP Id: rs200715932
MyVariant Identifiers: chrMT:g.8410C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8410C>T , J01415.2:m.8410C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.45C>T ENSP00000355265.1:p.Pro15=