Canonical Allele Identifier: CA913169572
Gene:

Linked Data

ClinVar Variation Id: 690141
ClinVar RCV Id: RCV000851023
dbSNP Id: rs1603223589

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12171A>G , J01415.2:m.12171A>G GRCh38