Canonical Allele Identifier: CA915952152
Gene:

Linked Data

ClinVar Variation Id: 690245
ClinVar RCV Id: RCV000851139
dbSNP Id: rs1603225604

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15937del , J01415.2:m.15937del GRCh38