Canonical Allele Identifier: CA120558

Gene:

Linked Data

• ClinVar Variation Id: 9586
• ClinVar RCV Id: RCV000010203 ; RCV000851084 ; RCV003153297
• dbSNP Id: rs121434462
• MyVariant Identifiers: chrMT:g.12315G>A (hg38)
• ERepo: CA120558/MONDO:0044970/014
• PubMed: PMID:8923013

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12315G>A , J01415.2:m.12315G>A	GRCh38