Canonical Allele Identifier: CA913177185
Gene:

Linked Data

ClinVar Variation Id: 690031
ClinVar RCV Id: RCV000850897
dbSNP Id: rs1603220981

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.7487C>T , J01415.2:m.7487C>T GRCh38