ClinGen Allele Registry
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Canonical Allele Identifier:
CA120564
Gene:
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.3252A>G
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000010217
RCV000850692
ClinVar Variation:
9594
dbSNP:
199474661
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.3252A>G , J01415.2:m.3252A>G
GRCh38
Search 100 bp 5'
Search 100 bp 3'