Canonical Allele Identifier: CA16603227
Gene:

Linked Data

ClinVar Variation Id: 376983
ClinVar RCV Id: RCV000426740 RCV000851017
dbSNP Id: rs376606918
MyVariant Identifiers: chrMT:g.12153C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12153C>T , J01415.2:m.12153C>T GRCh38
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