Canonical Allele Identifier: PA2825884658
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Thr38Ala
CA5958193
NM_001145266.1:c.112A>G