Canonical Allele Identifier: CA1573442180
Gene:

Linked Data

ClinVar Variation Id: 1014343
ClinVar RCV Id: RCV003538671
dbSNP Id: rs1750550359
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707345del , CM000667.2:g.112707345del GRCh38
NC_000005.9:g.112043042del , CM000667.1:g.112043042del GRCh37
NC_000005.8:g.112070941del NCBI36
NG_008481.4:g.19825del , LRG_130:g.19825del
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