Canonical Allele Identifier: CA131006
Gene:

Linked Data

ClinVar Variation Id: 42220
ClinVar RCV Id: RCV000035045 RCV000509092
dbSNP Id: rs2001030
MyVariant Identifiers: chrMT:g.1438A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1438A>G , J01415.2:m.1438A>G GRCh38
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