Allele Registry

Canonical Allele Identifier: PA2825971080

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV001250169

ClinVar Variation:

973538

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157749.1:p.Phe31del	CA602577840 NM_001164277.2:c.92_94del