Canonical Allele Identifier: PA219354
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68291
ClinVar RCV Id: RCV000059142 RCV000634548 RCV002477207
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Arg28Cys
CA219352
NM_001164277.2:c.82C>T