Allele Registry

Canonical Allele Identifier: PA284851

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000007330

RCV000059116

ClinVar Variation:

6921

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157749.1:p.Gly339Cys	CA284849 NM_001164277.2:c.1015G>T