Canonical Allele Identifier: CA913175135

Gene:

Linked Data

• ClinVar Variation Id: 690217
• ClinVar RCV Id: RCV000851109
• dbSNP Id: rs1603225570

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15893T>C , J01415.2:m.15893T>C	GRCh38