Allele Registry

Canonical Allele Identifier: PA2826466096

Gene: SLC38A9 HGNC NCBI

ClinVar RCV:

RCV004143382

ClinVar Variation:

2297301

HGVS (amino-acid)	Matching Registered Transcripts
NP_001245215.1:p.Leu57Phe	CA359760956 NM_001258286.1:c.171A>T CA359760957 NM_001258286.1:c.171A>C