Canonical Allele Identifier: CA2499217365
Gene:

Linked Data

ClinVar Variation Id: 1052288
ClinVar RCV Id: RCV003652209
dbSNP Id: rs2149627962
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.112707333del , CM000667.2:g.112707333del GRCh38
NC_000005.9:g.112043030del , CM000667.1:g.112043030del GRCh37
NC_000005.8:g.112070929del NCBI36
NG_008481.4:g.19813del , LRG_130:g.19813del
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