Allele Registry

Canonical Allele Identifier: PA219312

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000007332

RCV000059128

ClinVar Variation:

6923

HGVS (amino-acid)	Matching Registered Transcripts
NP_001458.1:p.Trp118Arg	CA219309 NM_001467.6:c.352T>C CA382904621 NM_001467.6:c.352T>A