Canonical Allele Identifier: CA120552
Gene:

Linked Data

ClinVar Variation Id: 9576
ClinVar RCV Id: RCV000010189 RCV000850644 RCV001804724 RCV002247290
dbSNP Id: rs387906420
MyVariant Identifiers: chrMT:g.616T>C (hg38)
ERepo: CA120552/MONDO:0044970/014
PubMed: PMID:20142618
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.616T>C , J01415.2:m.616T>C GRCh38
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