Canonical Allele Identifier: CA340921
Gene:

Linked Data

ClinVar Variation Id: 9565
ClinVar RCV Id: RCV000010179 RCV003162229
dbSNP Id: rs199474820
MyVariant Identifiers: chrMT:g.7510T>C (hg38)
ERepo: CA340921/MONDO:0044970/014
PubMed: PMID:10978361 PMID:20301595
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7510T>C , J01415.2:m.7510T>C GRCh38
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