Canonical Allele Identifier: CA414796222
Gene: MT-ATP8 HGNC NCBI

Linked Data

dbSNP Id: rs1603221500
MyVariant Identifiers: chrMT:g.8466A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8466A>C , J01415.2:m.8466A>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361851.1:c.101A>C ENSP00000355265.1:p.His34Pro