Canonical Allele Identifier: CA913180163
Gene:

Linked Data

ClinVar Variation Id: 689969
ClinVar RCV Id: RCV000850826
dbSNP Id: rs1553139251

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5663C>T , J01415.2:m.5663C>T GRCh38