Canonical Allele Identifier: CA913169476
Gene:

Linked Data

ClinVar Variation Id: 690129
ClinVar RCV Id: RCV000851009
dbSNP Id: rs1603223565

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12141A>G , J01415.2:m.12141A>G GRCh38