Canonical Allele Identifier: CA414795823
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692835
ClinVar RCV Id: RCV000854163
dbSNP Id: rs1603221431
MyVariant Identifiers: chrMT:g.8373A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8373A>T , J01415.2:m.8373A>T GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.8A>T ENSP00000355265.1:p.Gln3Leu
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