Canonical Allele Identifier: CA913177818

Gene:

Linked Data

• ClinVar Variation Id: 689890
• ClinVar RCV Id: RCV000850740
• dbSNP Id: rs1603219418

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4350C>T , J01415.2:m.4350C>T	GRCh38