Canonical Allele Identifier: CA130372
Gene:

Linked Data

ClinVar Variation Id: 39575
ClinVar RCV Id: RCV000032775 RCV000414832 RCV000791268
dbSNP Id: rs1556424691
MyVariant Identifiers: chrMT:g.15923A>G (hg38)
ERepo: CA130372/MONDO:0044970/014
PubMed: PMID:1379415 PMID:1645537 PMID:20301693
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15923A>G , J01415.2:m.15923A>G GRCh38
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