Allele Registry

Canonical Allele Identifier: PA2827651615

Gene: SLC19A1 HGNC NCBI

ClinVar Allele:

167450

ClinVar RCV:

RCV000144916

RCV001788041

RCV002055868

ClinVar Variation:

157588

HGVS (amino-acid)	Matching Registered Transcripts
NP_001339440.1:p.His27Arg	CA170984 NM_001352511.3:c.80A>G