Allele Registry

Canonical Allele Identifier: PA645408635

Gene: SLC19A3 HGNC NCBI

ClinVar Variation Id: 334879

HGVS (amino-acid)	Matching Registered Transcripts
NP_079519.1:p.Gly326Val	CA2149207 NM_025243.4:c.977G>T