Allele Registry

Canonical Allele Identifier: PA2825972033

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000059136

RCV000169286

ClinVar Variation:

68285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157751.1:p.Pro118Leu	CA219334 NM_001164279.2:c.353C>T