Canonical Allele Identifier: PA2825884448
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 304737
ClinVar RCV Id: RCV000334681 RCV002522197
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Thr38Ala
CA5958193
NM_001145265.2:c.112A>G