Canonical Allele Identifier: CA913169943

Gene:

Linked Data

• ClinVar Variation Id: 690180
• ClinVar RCV Id: RCV000851067
• dbSNP Id: rs1603223644

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12273A>G , J01415.2:m.12273A>G	GRCh38