Allele Registry

Canonical Allele Identifier: PA219357

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000059143

RCV000169410

ClinVar Variation:

68292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157749.1:p.Ile278Asn	CA219355 NM_001164277.2:c.833T>A