Canonical Allele Identifier: CA337098672
Gene:

Linked Data

ClinVar Variation Id: 690104
ClinVar RCV Id: RCV000850982 RCV002221589
dbSNP Id: rs41347846
MyVariant Identifiers: chrMT:g.10034T>C (hg38)
ERepo: CA337098672/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10034T>C , J01415.2:m.10034T>C GRCh38
Search 100 bp 5'
Search 100 bp 3'