Canonical Allele Identifier: CA913179744
Gene:

Linked Data

ClinVar Variation Id: 689925
ClinVar RCV Id: RCV000850778
dbSNP Id: rs1603220004

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5524T>C , J01415.2:m.5524T>C GRCh38