ClinGen Allele Registry
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Canonical Allele Identifier:
CA337100567
Gene:
Linked Data - Variant Effect Evidence
MyVariant.info:
GRCh38
chrMT:g.15904C>T
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000851116
ClinVar Variation:
690224
dbSNP:
35788393
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.15904C>T , J01415.2:m.15904C>T
GRCh38
Search 100 bp 5'
Search 100 bp 3'