Canonical Allele Identifier: PA2825884679
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2006680
ClinVar RCV Id: RCV002811874
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Leu78Phe
CA380202633
NM_001145266.1:c.232C>T