Canonical Allele Identifier: CA913178263
Gene:

Linked Data

ClinVar Variation Id: 689920
ClinVar RCV Id: RCV000850772
dbSNP Id: rs1603219466

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4464G>A , J01415.2:m.4464G>A GRCh38