Canonical Allele Identifier: CA913171839

Gene:

Linked Data

• ClinVar Variation Id: 690205
• ClinVar RCV Id: RCV000851095
• dbSNP Id: rs1556424481

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14696A>G , J01415.2:m.14696A>G	GRCh38