Canonical Allele Identifier: CA131014
Gene:

Linked Data

ClinVar Variation Id: 42229
dbSNP Id: rs397515728
MyVariant Identifiers: chrMT:g.7493C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7493C>T , J01415.2:m.7493C>T GRCh38