Canonical Allele Identifier: CA120579

Gene:

Linked Data

• ClinVar Variation Id: 9614
• ClinVar RCV Id: RCV000010238
• dbSNP Id: rs199476140
• PubMed: PMID:10996779

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4369dup , J01415.2:m.4369dup	GRCh38