Canonical Allele Identifier: CA10581287
Gene:

Linked Data

ClinVar Variation Id: 235361
dbSNP Id: rs376062400
MyVariant Identifiers: chrMT:g.12239C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12239C>T , J01415.2:m.12239C>T GRCh38