Canonical Allele Identifier: CA414802370
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 693119
ClinVar RCV Id: RCV000854470
dbSNP Id: rs1556423629
MyVariant Identifiers: chrMT:g.9182G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.9182G>A , J01415.2:m.9182G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.656G>A ENSP00000354632.2:p.Ser219Asn
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