Canonical Allele Identifier: CA915952145
Gene:

Linked Data

ClinVar Variation Id: 690170
ClinVar RCV Id: RCV000851057
dbSNP Id: rs1603223633

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12241dup , J01415.2:m.12241dup GRCh38