Canonical Allele Identifier: PA2825884697
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 965658
ClinVar RCV Id: RCV001240162

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Ile112Met
CA380202843
NM_001145266.1:c.336C>G