Canonical Allele Identifier: CA913179055
Gene:

Linked Data

ClinVar Variation Id: 690080
ClinVar RCV Id: RCV000850955
dbSNP Id: rs1603221418

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.8349C>T , J01415.2:m.8349C>T GRCh38