Canonical Allele Identifier: CA913169907

Gene:

Linked Data

• ClinVar Variation Id: 690178
• ClinVar RCV Id: RCV000851065
• dbSNP Id: rs1603223642

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12264C>T , J01415.2:m.12264C>T	GRCh38