Canonical Allele Identifier: CA913169612

Gene:

Linked Data

• ClinVar Variation Id: 690147
• ClinVar RCV Id: RCV000851030
• dbSNP Id: rs1603223598

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12181C>T , J01415.2:m.12181C>T	GRCh38