Canonical Allele Identifier: CA2499216389

Gene:

Linked Data

• ClinVar Variation Id: 997766
• ClinVar RCV Id: RCV001293323

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10148615_10158450del , CM000665.2:g.10148615_10158450del	GRCh38
NC_000003.11:g.10190299_10200134del , CM000665.1:g.10190299_10200134del	GRCh37
NC_000003.10:g.10165299_10175134del	NCBI36