Canonical Allele Identifier: CA913175346

Gene:

Linked Data

• ClinVar Variation Id: 690263
• ClinVar RCV Id: RCV000851161
• dbSNP Id: rs1603225620

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.15976T>C , J01415.2:m.15976T>C	GRCh38