Canonical Allele Identifier: PA093287
Gene: SLC19A3 HGNC NCBI

Linked Data

ClinVar Variation Id: 4563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_079519.1:p.Thr422Ala
CA253227
NM_025243.4:c.1264A>G