Canonical Allele Identifier: CA913169137
Gene:

Linked Data

ClinVar Variation Id: 930602
ClinVar RCV Id: RCV001196387
dbSNP Id: rs199474665

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3290T>A , J01415.2:m.3290T>A GRCh38