Canonical Allele Identifier: CA913163121

Gene:

Linked Data

• ClinVar Variation Id: 689834
• ClinVar RCV Id: RCV000850662
• dbSNP Id: rs1603218582

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.1608G>A , J01415.2:m.1608G>A	GRCh38