Canonical Allele Identifier: CA913175479

Gene:

Linked Data

• ClinVar Variation Id: 690277
• ClinVar RCV Id: RCV000851175
• dbSNP Id: rs1603225641

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.16021C>T , J01415.2:m.16021C>T	GRCh38