Canonical Allele Identifier: CA913177787
Gene:

Linked Data

ClinVar Variation Id: 689887
ClinVar RCV Id: RCV000850737
dbSNP Id: rs1603219415

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4339G>A , J01415.2:m.4339G>A GRCh38