Canonical Allele Identifier: CA913169888
Gene:

Linked Data

ClinVar Variation Id: 690177
ClinVar RCV Id: RCV000851064
dbSNP Id: rs118203888

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12258C>T , J01415.2:m.12258C>T GRCh38