Canonical Allele Identifier: CA913169972

Gene:

Linked Data

• ClinVar Variation Id: 690186
• ClinVar RCV Id: RCV000851073
• dbSNP Id: rs1603223651

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12281C>T , J01415.2:m.12281C>T	GRCh38