Canonical Allele Identifier: CA913180626

Gene:

Linked Data

• ClinVar Variation Id: 690012
• ClinVar RCV Id: RCV000850870
• dbSNP Id: rs1603220149

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5840C>A , J01415.2:m.5840C>A	GRCh38