Canonical Allele Identifier: CA915952154
Gene:

Linked Data

ClinVar Variation Id: 690276
ClinVar RCV Id: RCV000851174
dbSNP Id: rs1603225639
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.16018_16032dup , J01415.2:m.16018_16032dup GRCh38
Search 100 bp 5'
Search 100 bp 3'