Canonical Allele Identifier: CA10581287
Gene:

Linked Data

ClinVar Variation Id: 235361
ClinVar RCV Id: RCV000224786 RCV000851055 RCV002221520
dbSNP Id: rs376062400
MyVariant Identifiers: chrMT:g.12239C>T (hg38)
ERepo: CA10581287/MONDO:0044970/014
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Genomic Alleles

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