Canonical Allele Identifier: CA913177903

Gene:

Linked Data

• ClinVar Variation Id: 689894
• ClinVar RCV Id: RCV000850745
• dbSNP Id: rs1603219428

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.4371T>C , J01415.2:m.4371T>C	GRCh38