Allele Registry

Canonical Allele Identifier: PA2827491767

Gene: SLC38A9 HGNC NCBI

ClinVar RCV:

RCV004143382

ClinVar Variation:

2297301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001336313.1:p.Leu120Phe	CA359760956 NM_001349384.1:c.360A>T CA359760957 NM_001349384.1:c.360A>C