Canonical Allele Identifier: PA2825884688
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1949767
ClinVar RCV Id: RCV002676467
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Arg102His
CA5958227
NM_001145266.1:c.305G>A