ClinGen Allele Registry
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Canonical Allele Identifier:
CA337095950
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.825T>A
Linked Data - NCBI & NCI
dbSNP:
2853520
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.825T>A , J01415.2:m.825T>A
GRCh38
Search 100 bp 5'
Search 100 bp 3'