Canonical Allele Identifier: PA2825884441
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Leu26Ser
CA5958187
NM_001145265.2:c.77T>C