Canonical Allele Identifier: CA913177669
Gene:

Linked Data

ClinVar Variation Id: 618731
ClinVar RCV Id: RCV000757492
dbSNP Id: rs1569483932

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4305A>G , J01415.2:m.4305A>G GRCh38