Canonical Allele Identifier: CA337097843
Gene: MT-ATP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 692840
ClinVar RCV Id: RCV000854169
dbSNP Id: rs879199176
MyVariant Identifiers: chrMT:g.8388T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8388T>C , J01415.2:m.8388T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361851.1:c.23T>C ENSP00000355265.1:p.Val8Ala
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