Allele Registry

Canonical Allele Identifier: PA915985199

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000671757

ClinVar Variation:

555851

HGVS (amino-acid)	Matching Registered Transcripts
NP_001458.1:p.Phe31Leu	CA229600928 NM_001467.6:c.93C>G CA382908421 NM_001467.6:c.93C>A CA382908439 NM_001467.6:c.91T>C