Canonical Allele Identifier: CA2580102079

Gene:

Linked Data

• ClinVar Variation Id: 1806456
• ClinVar RCV Id: RCV003223355

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.10950_15540del , J01415.2:m.10950_15540del	GRCh38