Canonical Allele Identifier: CA913169703

Gene:

Linked Data

• ClinVar Variation Id: 690157
• ClinVar RCV Id: RCV000851042
• dbSNP Id: rs1603223615

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12205C>T , J01415.2:m.12205C>T	GRCh38