Canonical Allele Identifier: CA913180629

Gene:

Linked Data

• ClinVar Variation Id: 690014
• ClinVar RCV Id: RCV000850872
• dbSNP Id: rs1603220150

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5841T>C , J01415.2:m.5841T>C	GRCh38