Canonical Allele Identifier: CA913180613

Gene:

Linked Data

• ClinVar Variation Id: 690010
• ClinVar RCV Id: RCV000850868
• dbSNP Id: rs1603220147

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5837G>A , J01415.2:m.5837G>A	GRCh38