Allele Registry

Canonical Allele Identifier: PA2827491676

Gene: SLC38A9 HGNC NCBI

ClinVar RCV:

RCV004143382

ClinVar Variation:

2297301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336311.1:p.Leu120Phe	CA359760956 NM_001349382.1:c.360A>T CA359760957 NM_001349382.1:c.360A>C