Canonical Allele Identifier: CA915952144
Gene:

Linked Data

ClinVar Variation Id: 690169
ClinVar RCV Id: RCV000851056 RCV001250990 RCV003985435
dbSNP Id: rs1603223633
ERepo: CA915952144/MONDO:0044970/014
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Genomic Alleles

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