Canonical Allele Identifier: CA913163351
Gene:

Linked Data

ClinVar Variation Id: 690125
ClinVar RCV Id: RCV000851005
dbSNP Id: rs1603222845

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10457T>C , J01415.2:m.10457T>C GRCh38