Canonical Allele Identifier: CA913180686

Gene:

Linked Data

• ClinVar Variation Id: 690018
• ClinVar RCV Id: RCV000850877
• dbSNP Id: rs1603220157

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5858T>C , J01415.2:m.5858T>C	GRCh38