Allele Registry

Canonical Allele Identifier: PA219281

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000059118

RCV000288403

ClinVar Variation:

21298

HGVS (amino-acid)	Matching Registered Transcripts
NP_001458.1:p.Ala367Thr	CA219278 NM_001467.6:c.1099G>A