Canonical Allele Identifier: CA913169005

Gene:

Linked Data

• ClinVar Variation Id: 689859
• ClinVar RCV Id: RCV000850694
• dbSNP Id: rs1603218855

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.3254C>T , J01415.2:m.3254C>T	GRCh38