Canonical Allele Identifier: CA913175242
Gene:

Linked Data

ClinVar Variation Id: 690242
ClinVar RCV Id: RCV000851136
dbSNP Id: rs1556424699

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15935A>G , J01415.2:m.15935A>G GRCh38