Canonical Allele Identifier: CA913169075
Gene:

Linked Data

ClinVar Variation Id: 689865
ClinVar RCV Id: RCV000850702
dbSNP Id: rs1603218865

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3272T>C , J01415.2:m.3272T>C GRCh38