Canonical Allele Identifier: CA120549
Gene:

Linked Data

ClinVar Variation Id: 9570
ClinVar RCV Id: RCV000010183 RCV003162230
dbSNP Id: rs199474699
MyVariant Identifiers: chrMT:g.15990C>T (hg38)
ERepo: CA120549/MONDO:0044970/014
PubMed: PMID:7689388
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15990C>T , J01415.2:m.15990C>T GRCh38
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