Allele Registry

Canonical Allele Identifier: PA3057721203

Gene: SLC19A2 HGNC NCBI

ClinVar RCV:

RCV005409503

ClinVar Variation:

3896598

HGVS (amino-acid)	Matching Registered Transcripts
NP_008927.1:p.Gly172Val	CA343110319 NM_006996.3:c.515G>T