Canonical Allele Identifier: CA913169655

Gene:

Linked Data

• ClinVar Variation Id: 690153
• ClinVar RCV Id: RCV000851037
• dbSNP Id: rs1603223611

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12193A>G , J01415.2:m.12193A>G	GRCh38