Canonical Allele Identifier: CA913179047
Gene:

Linked Data

ClinVar Variation Id: 690077
ClinVar RCV Id: RCV000850952
dbSNP Id: rs1603221415

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8346C>A , J01415.2:m.8346C>A GRCh38