Canonical Allele Identifier: CA913179100
Gene:

Linked Data

ClinVar Variation Id: 690084
ClinVar RCV Id: RCV000850960
dbSNP Id: rs1603221423

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8362T>G , J01415.2:m.8362T>G GRCh38