Canonical Allele Identifier: CA913175262
Gene:

Linked Data

ClinVar Variation Id: 690255
ClinVar RCV Id: RCV000851150
dbSNP Id: rs1603225608

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15944T>C , J01415.2:m.15944T>C GRCh38