Canonical Allele Identifier: CA2499216387

Gene:

Linked Data

• ClinVar Variation Id: 997765
• ClinVar RCV Id: RCV001293322

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.10148566_10158401del , CM000665.2:g.10148566_10158401del	GRCh38
NC_000003.11:g.10190250_10200085del , CM000665.1:g.10190250_10200085del	GRCh37
NC_000003.10:g.10165250_10175085del	NCBI36