Allele Registry

Canonical Allele Identifier: PA915988080

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000059118

RCV000288403

ClinVar Variation:

21298

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157750.1:p.Ala389Thr	CA219278 NM_001164278.2:c.1165G>A