Canonical Allele Identifier: CA337097898
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692872
ClinVar RCV Id: RCV000854202
dbSNP Id: rs201902227
MyVariant Identifiers: chrMT:g.8478C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8478C>T , J01415.2:m.8478C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.113C>T ENSP00000355265.1:p.Ser38Leu
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