Canonical Allele Identifier: CA913175185
Gene:

Linked Data

ClinVar Variation Id: 690231
ClinVar RCV Id: RCV000851123
dbSNP Id: rs1603225584

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15913C>T , J01415.2:m.15913C>T GRCh38