Canonical Allele Identifier: CA913175248
Gene:

Linked Data

ClinVar Variation Id: 690247
ClinVar RCV Id: RCV000851141
dbSNP Id: rs1603225605

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15937A>G , J01415.2:m.15937A>G GRCh38