Allele Registry

Canonical Allele Identifier: PA219345

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000059139

RCV000169003

ClinVar Variation:

68288

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157749.1:p.Tyr24His	CA219343 NM_001164277.2:c.70T>C