Canonical Allele Identifier: CA414795970
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692846
ClinVar RCV Id: RCV000854176
dbSNP Id: rs1556423448
MyVariant Identifiers: chrMT:g.8406C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8406C>T , J01415.2:m.8406C>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.41C>T ENSP00000355265.1:p.Thr14Ile
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