Allele Registry

Canonical Allele Identifier: PA219336

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000059136

RCV000169286

ClinVar Variation:

68285

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157749.1:p.Pro191Leu	CA219334 NM_001164277.2:c.572C>T