Allele Registry

Canonical Allele Identifier: PA658832766

Gene: SLC37A4 HGNC NCBI

ClinVar RCV:

RCV000673600

ClinVar Variation:

557457

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157749.1:p.Gly276Ala	CA382900260 NM_001164277.2:c.827G>C