Canonical Allele Identifier: CA913178085
Gene:

Linked Data

ClinVar Variation Id: 689910
ClinVar RCV Id: RCV000850762
dbSNP Id: rs1556422856

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4418T>C , J01415.2:m.4418T>C GRCh38