Allele Registry

Canonical Allele Identifier: PA219366

Gene: SLC37A4 HGNC NCBI

ClinVar Allele:

79185

ClinVar RCV:

RCV000059146

RCV001388583

RCV001813754

RCV002498349

ClinVar Variation:

68294

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157749.1:p.Arg300His	CA219364 NM_001164277.2:c.899G>A