Allele Registry

Canonical Allele Identifier: PA2825972299

Gene: SLC37A4 HGNC NCBI

ClinVar Variation Id: 554828

ClinVar RCV Id: RCV000670525

ClinVar Variation Id: 1366825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157751.1:p.Ser319Arg	CA6311601 NM_001164279.2:c.957T>G CA382894369 NM_001164279.2:c.957T>A CA382894379 NM_001164279.2:c.955A>C