Canonical Allele Identifier: CA2573105433

Gene:

Linked Data

• ClinVar Variation Id: 1525973
• ClinVar RCV Id: RCV002037090
• dbSNP Id: rs2124599393

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.16159C>A , J01415.2:m.16159C>A	GRCh38