Canonical Allele Identifier: PA2825971298
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2189722
ClinVar RCV Id: RCV002611772
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Tyr265His
CA382900590
NM_001164277.2:c.793T>C