Canonical Allele Identifier: PA2825971654
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68280
ClinVar RCV Id: RCV000059131 RCV001204831
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Gly149Glu
CA219319
NM_001164278.2:c.446G>A