Canonical Allele Identifier: CA913177799
Gene:

Linked Data

ClinVar Variation Id: 689889
ClinVar RCV Id: RCV000850739
dbSNP Id: rs386828939

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4343A>G , J01415.2:m.4343A>G GRCh38