Canonical Allele Identifier: CA913177719
Gene:

Linked Data

ClinVar Variation Id: 689884
ClinVar RCV Id: RCV000850733
dbSNP Id: rs1603219406

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4320C>A , J01415.2:m.4320C>A GRCh38