Canonical Allele Identifier: CA913180005
Gene:

Linked Data

ClinVar Variation Id: 1684909
ClinVar RCV Id: RCV002248001
dbSNP Id: rs2124593028

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5613T>C , J01415.2:m.5613T>C GRCh38