Allele Registry

Canonical Allele Identifier: PA2825972091

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000007342

ClinVar Variation:

6930

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157751.1:p.Val163del	CA254002 NM_001164279.2:c.487_489del