Allele Registry

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Canonical Allele Identifier: PA2825972931

Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1411318

ClinVar RCV Id: RCV001942933 RCV002478373

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Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001157752.1:p.Glu429Asp	CA382893109 NM_001164280.2:c.1287G>T CA382893118 NM_001164280.2:c.1287G>C