Canonical Allele Identifier: PA2825884648
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 566519

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Gly17Arg
CA5958182
NM_001145266.1:c.49G>A
CA5958183
NM_001145266.1:c.49G>C