Canonical Allele Identifier: CA913180261
Gene:

Linked Data

ClinVar Variation Id: 689976
ClinVar RCV Id: RCV000850833
dbSNP Id: rs1603220092

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5693T>C , J01415.2:m.5693T>C GRCh38