Canonical Allele Identifier: CA340922
Gene:

Linked Data

ClinVar Variation Id: 9566
ClinVar RCV Id: RCV000010180 RCV000850906 RCV002247287 RCV003153295
dbSNP Id: rs199474821
MyVariant Identifiers: chrMT:g.7511T>C (hg38)
ERepo: CA340922/MONDO:0044970/014
PubMed: PMID:10340654 PMID:10371545 PMID:12461693 PMID:20301595
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7511T>C , J01415.2:m.7511T>C GRCh38
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