Canonical Allele Identifier: CA913169744

Gene:

Linked Data

• ClinVar Variation Id: 690160
• ClinVar RCV Id: RCV000851045
• dbSNP Id: rs1603223618

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12216C>T , J01415.2:m.12216C>T	GRCh38