ClinGen Allele Registry
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Canonical Allele Identifier:
CA120567
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.3290T>C
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000010220
RCV000850710
ClinVar Variation:
9597
dbSNP:
199474665
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.3290T>C , J01415.2:m.3290T>C
GRCh38
Search 100 bp 5'
Search 100 bp 3'