Canonical Allele Identifier: CA270625

Gene:

Linked Data

• ClinVar Variation Id: 143918
• ClinVar RCV Id: RCV000133449
• dbSNP Id: rs527236202
• MyVariant Identifiers: chrMT:g.14732A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14732A>G , J01415.2:m.14732A>G	GRCh38