Canonical Allele Identifier: CA913169860

Gene:

Linked Data

• ClinVar Variation Id: 690175
• ClinVar RCV Id: RCV000851062
• dbSNP Id: rs1603223639

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12250C>T , J01415.2:m.12250C>T	GRCh38