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)
• PubMed: PMID:1379415 ; PMID:1645537 ; PMID:20301693
• ERepo: CA130372/MONDO:0044970/014

Genomic Alleles

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