Canonical Allele Identifier: CA913169631

Gene:

Linked Data

• ClinVar Variation Id: 918020
• ClinVar RCV Id: RCV001175267
• dbSNP Id: rs2068730503

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.12187C>T , J01415.2:m.12187C>T	GRCh38