Canonical Allele Identifier: CA913180137
Gene:

Linked Data

ClinVar Variation Id: 689965
ClinVar RCV Id: RCV000850822
dbSNP Id: rs1603220072

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5654T>C , J01415.2:m.5654T>C GRCh38