Allele Registry

Canonical Allele Identifier: PA103436

Gene: SLC35C1 HGNC NCBI

ClinVar RCV:

RCV000005005

ClinVar Variation:

4739

HGVS (amino-acid)	Matching Registered Transcripts
NP_060859.4:p.Arg147Cys	CA253271 NM_018389.5:c.439C>T