Canonical Allele Identifier: CA262598311
Gene:

Linked Data

ClinVar Variation Id: 1168490
ClinVar RCV Id: RCV001518793
dbSNP Id: rs148370307

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73136378del , CM000676.2:g.73136378del GRCh38
NC_000014.8:g.73603086del , CM000676.1:g.73603086del GRCh37
NC_000014.7:g.72672839del NCBI36
NG_007386.2:g.4908del