Allele Registry

Canonical Allele Identifier: PA2825971779

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000169082

RCV000300702

ClinVar Variation:

188762

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157750.1:p.Gln248Ter