Canonical Allele Identifier: CA915943565
Gene:

Linked Data

ClinVar Variation Id: 652540
ClinVar RCV Id: RCV003653369
dbSNP Id: rs1580995299
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707353dup , CM000667.2:g.112707353dup GRCh38
NC_000005.9:g.112043050dup , CM000667.1:g.112043050dup GRCh37
NC_000005.8:g.112070949dup NCBI36
NG_008481.4:g.19833dup , LRG_130:g.19833dup
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