Canonical Allele Identifier: CA10577185
Gene:

Linked Data

ClinVar Variation Id: 228859
ClinVar RCV Id: RCV000218791 RCV000850905 RCV003319188
dbSNP Id: rs876657868
MyVariant Identifiers: chrMT:g.7502C>T (hg38)
ERepo: CA10577185/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7502C>T , J01415.2:m.7502C>T GRCh38
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