Canonical Allele Identifier: CA913169600

Gene:

Linked Data

• ClinVar Variation Id: 690146
• ClinVar RCV Id: RCV000851029
• dbSNP Id: rs1603223596

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12178C>T , J01415.2:m.12178C>T	GRCh38