Canonical Allele Identifier: CA913177957
Gene:

Linked Data

ClinVar Variation Id: 689900
ClinVar RCV Id: RCV000850751
dbSNP Id: rs1603219436

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4384T>A , J01415.2:m.4384T>A GRCh38