Canonical Allele Identifier: CA309472568
Gene:

Linked Data

dbSNP Id: rs103294
MyVariant Identifiers: chr19:g.54293995T>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.54293995T>C , CM000681.2:g.54293995T>C GRCh38