Allele Registry

Canonical Allele Identifier: PA916013606

Gene: SLC35A2 HGNC NCBI

ClinVar Allele:

438444

ClinVar RCV:

RCV000513019

RCV001511787

ClinVar Variation:

444804

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269576.1:p.Ser150Asn	CA10406070 NM_001282647.2:c.449G>A