Canonical Allele Identifier: CA913171809

Gene:

Linked Data

• ClinVar Variation Id: 690200
• ClinVar RCV Id: RCV000851090
• dbSNP Id: rs1603224831

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14684C>T , J01415.2:m.14684C>T	GRCh38