Canonical Allele Identifier: CA913180707

Gene:

Linked Data

• ClinVar Variation Id: 690020
• ClinVar RCV Id: RCV000850879
• dbSNP Id: rs1603220159

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.5865T>C , J01415.2:m.5865T>C	GRCh38