Allele Registry

Canonical Allele Identifier: PA2825972394

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV003087309

ClinVar Variation:

2172207

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157752.1:p.Thr30Ile	CA382908448 NM_001164280.2:c.89C>T