Canonical Allele Identifier: CA703671921
Gene:

Linked Data

dbSNP Id: rs2904622
MyVariant Identifiers: chr14:g.106768250C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.106768250C>T , CM000676.2:g.106768250C>T GRCh38