Allele Registry

Canonical Allele Identifier: PA915985195

Gene: SLC37A4 HGNC NCBI

ClinVar Variation Id: 68291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001458.1:p.Arg28Cys	CA219352 NM_001467.6:c.82C>T