Canonical Allele Identifier: PA2825884438
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 566519
ClinVar RCV Id: RCV000686350 RCV002544746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Gly17Arg
CA5958182
NM_001145265.2:c.49G>A
CA5958183
NM_001145265.2:c.49G>C