Canonical Allele Identifier: CA913180234
Gene:

Linked Data

ClinVar Variation Id: 689975
ClinVar RCV Id: RCV000850832
dbSNP Id: rs1603220088

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5686A>T , J01415.2:m.5686A>T GRCh38