ClinGen Allele Registry
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Canonical Allele Identifier:
CA344658
Gene:
Linked Data
ClinVar Variation Id:
42212
ClinVar RCV Id:
RCV000035037
RCV000992377
dbSNP Id:
rs28358572
MyVariant Identifiers:
chrMT:g.1243T>C (hg38)
PubMed:
PMID:11245424
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.1243T>C , J01415.2:m.1243T>C
GRCh38
Search 100 bp 5'
Search 100 bp 3'