ClinGen Allele Registry
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Canonical Allele Identifier:
CA337100622
Gene:
Linked Data
ClinVar Variation Id:
690265
ClinVar RCV Id:
RCV000851163
dbSNP Id:
rs201041059
MyVariant Identifiers:
chrMT:g.15978C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.15978C>T , J01415.2:m.15978C>T
GRCh38
Search 100 bp 5'
Search 100 bp 3'