Canonical Allele Identifier: CA913178082
Gene:

Linked Data

ClinVar Variation Id: 689909
ClinVar RCV Id: RCV000850761
dbSNP Id: rs1603219452

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4417A>G , J01415.2:m.4417A>G GRCh38