Allele Registry

Canonical Allele Identifier: PA645502827

Gene: SLC35C1 HGNC NCBI

ClinVar Variation Id: 304736

HGVS (amino-acid)	Matching Registered Transcripts
NP_060859.4:p.Arg10Lys	CA5958169 NM_018389.5:c.29G>A