Canonical Allele Identifier: CA913179986
Gene:

Linked Data

ClinVar Variation Id: 689956
ClinVar RCV Id: RCV000850813
dbSNP Id: rs1603220054

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5607T>C , J01415.2:m.5607T>C GRCh38