Allele Registry

Canonical Allele Identifier: PA2825971719

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV003069970

ClinVar Variation:

2158838

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157750.1:p.Asn198Ser	CA6311805 NM_001164278.2:c.593A>G