Canonical Allele Identifier: CA913169503
Gene:

Linked Data

ClinVar Variation Id: 690134
ClinVar RCV Id: RCV000851015
dbSNP Id: rs1603223574

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.12150T>C , J01415.2:m.12150T>C GRCh38