Canonical Allele Identifier: CA913179979
Gene:

Linked Data

ClinVar Variation Id: 689954
ClinVar RCV Id: RCV000850811
dbSNP Id: rs1603220053

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5604C>T , J01415.2:m.5604C>T GRCh38