Canonical Allele Identifier: CA913180627

Gene:

Linked Data

• ClinVar Variation Id: 690013
• ClinVar RCV Id: RCV000850871
• dbSNP Id: rs1603220149

Genomic Alleles

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