Allele Registry

Canonical Allele Identifier: PA2825971491

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000665062

ClinVar Variation:

550340

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157750.1:p.Phe33Leu	CA382908363 NM_001164278.2:c.99T>G CA382908364 NM_001164278.2:c.99T>A CA382908380 NM_001164278.2:c.97T>C