Canonical Allele Identifier: CA913161497
Gene:

Linked Data

ClinVar Variation Id: 690094
ClinVar RCV Id: RCV000850971
dbSNP Id: rs1603222622

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10006A>G , J01415.2:m.10006A>G GRCh38