Canonical Allele Identifier: PA2825884468
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1345882
ClinVar RCV Id: RCV002037619

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Leu74Pro
CA380202607
NM_001145265.2:c.221T>C