Canonical Allele Identifier: PA2825884835
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440591
ClinVar RCV Id: RCV001967706
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Pro336Leu
CA5958387
NM_001145266.1:c.1007C>T