Allele Registry

Canonical Allele Identifier: PA2825972134

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000669863

ClinVar Variation:

554262

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157751.1:p.Val202Ile	CA382900314 NM_001164279.2:c.604G>A