Canonical Allele Identifier: PA2825884516
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1349556
ClinVar RCV Id: RCV002051103
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Gly166Arg
CA5958261
NM_001145265.2:c.496G>A
CA380203681
NM_001145265.2:c.496G>C