Allele Registry

Canonical Allele Identifier: PA2580181813

Gene: SLC38A9 HGNC NCBI

ClinVar RCV:

RCV004143382

ClinVar Variation:

2297301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245216.1:p.Leu93Phe	CA359760956 NM_001258287.1:c.279A>T CA359760957 NM_001258287.1:c.279A>C