Canonical Allele Identifier: CA120563
Gene:

Linked Data

ClinVar Variation Id: 9593
ClinVar RCV Id: RCV000010216 RCV000850690
dbSNP Id: rs199474664
MyVariant Identifiers: chrMT:g.3250T>C (hg38)
PubMed: PMID:1514779 PMID:9003864
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3250T>C , J01415.2:m.3250T>C GRCh38
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