Canonical Allele Identifier: CA913169803

Gene:

Linked Data

• ClinVar Variation Id: 690166
• ClinVar RCV Id: RCV000851051
• dbSNP Id: rs1603223628

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12234A>G , J01415.2:m.12234A>G	GRCh38