ClinGen Allele Registry
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Canonical Allele Identifier:
CA120588
Gene:
Linked Data
ClinVar Variation Id:
9626
ClinVar RCV Id:
RCV000010252
dbSNP Id:
rs199474823
COSMIC:
COSN1085345
COSN1085346
COSN1085347
COSN1085348
MyVariant Identifiers:
chrMT:g.2991T>C (hg38)
PubMed:
PMID:6273808
PMID:7219548
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_012920.1:m.2991T>C , J01415.2:m.2991T>C
GRCh38
Search 100 bp 5'
Search 100 bp 3'