Canonical Allele Identifier: CA915952048

Gene:

Linked Data

• ClinVar Variation Id: 638147
• ClinVar RCV Id: RCV000790615

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.8350_13450del , J01415.2:m.8350_13450del	GRCh38