Canonical Allele Identifier: CA913178213
Gene:

Linked Data

ClinVar Variation Id: 689914
ClinVar RCV Id: RCV000850766
dbSNP Id: rs1603219461

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4451T>G , J01415.2:m.4451T>G GRCh38