Canonical Allele Identifier: CA913169003

Gene:

Linked Data

• ClinVar Variation Id: 689860
• ClinVar RCV Id: RCV000850695
• dbSNP Id: rs1603218855

Genomic Alleles

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