Allele Registry

Canonical Allele Identifier: PA915985559

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000669863

ClinVar Variation:

554262

HGVS (amino-acid)	Matching Registered Transcripts
NP_001458.1:p.Val275Ile	CA382900314 NM_001467.6:c.823G>A