Canonical Allele Identifier: PA916066070
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 723737
ClinVar RCV Id: RCV001106358 RCV002540158
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Val76Ile
CA5958206
NM_018389.5:c.226G>A