Canonical Allele Identifier: CA915952199

Gene:

Linked Data

• ClinVar Variation Id: 689881
• ClinVar RCV Id: RCV000850727
• dbSNP Id: rs1603219400

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4314del , J01415.2:m.4314del	GRCh38