Allele Registry

Canonical Allele Identifier: PA2825971808

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV001887568

ClinVar Variation:

1397113

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157750.1:p.Val275Gly	CA382900287 NM_001164278.2:c.824T>G