Allele Registry

Canonical Allele Identifier: PA2580338859

Gene: SLC19A2 HGNC NCBI

ClinVar RCV:

RCV003069107

ClinVar Variation:

2154103

HGVS (amino-acid)	Matching Registered Transcripts
NP_008927.1:p.Trp250Cys	CA1233018 NM_006996.3:c.750G>C CA343109823 NM_006996.3:c.750G>T