Canonical Allele Identifier: CA913171839
Gene:

Linked Data

ClinVar Variation Id: 690205
ClinVar RCV Id: RCV000851095
dbSNP Id: rs1556424481

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14696A>G , J01415.2:m.14696A>G GRCh38