Canonical Allele Identifier: PA2825971962
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 553918
ClinVar RCV Id: RCV000669458
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Phe20Tyr
CA382905325
NM_001164279.2:c.59T>A