Canonical Allele Identifier: CA120537
Gene:

Linked Data

ClinVar Variation Id: 9549
ClinVar RCV Id: RCV000010157 RCV000010158 RCV000850667
dbSNP Id: rs199476144
MyVariant Identifiers: chrMT:g.1624C>T (hg38)
PubMed: PMID:11799391 PMID:20301352
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1624C>T , J01415.2:m.1624C>T GRCh38
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