Canonical Allele Identifier: CA414795879
Gene: MT-ATP8 HGNC NCBI

Linked Data

dbSNP Id: rs1556423439
MyVariant Identifiers: chrMT:g.8387G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8387G>T , J01415.2:m.8387G>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361851.1:c.22G>T ENSP00000355265.1:p.Val8Leu
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