Canonical Allele Identifier: CA913163288
Gene:

Linked Data

ClinVar Variation Id: 689839
ClinVar RCV Id: RCV000850669
dbSNP Id: rs1603218587

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.1629A>G , J01415.2:m.1629A>G GRCh38