Allele Registry

Canonical Allele Identifier: PA645466164

Gene: SLC35A2 HGNC NCBI

ClinVar Allele:

266848

ClinVar RCV:

RCV000377201

RCV002429215

RCV002521886

ClinVar Variation:

282611

HGVS (amino-acid)	Matching Registered Transcripts
NP_005651.1:p.Leu276Phe	CA10406092 NM_005660.3:c.826C>T