Canonical Allele Identifier: CA913180668

Gene:

Linked Data

• ClinVar Variation Id: 690016
• ClinVar RCV Id: RCV000850875
• dbSNP Id: rs1603220153

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5852T>C , J01415.2:m.5852T>C	GRCh38