Canonical Allele Identifier: CA913180459
Gene:

Linked Data

ClinVar Variation Id: 689991
ClinVar RCV Id: RCV000850849
dbSNP Id: rs1556423033

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5788T>C , J01415.2:m.5788T>C GRCh38