Canonical Allele Identifier: CA414796877
Gene: MT-ATP6 HGNC NCBI

Linked Data

ClinVar Variation Id: 692920
ClinVar RCV Id: RCV000854255
dbSNP Id: rs1556423501
MyVariant Identifiers: chrMT:g.8602T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8602T>C , J01415.2:m.8602T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361899.2:c.76T>C ENSP00000354632.2:p.Phe26Leu
Search 100 bp 5'
Search 100 bp 3'