Canonical Allele Identifier: PA219366
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68294
ClinVar RCV Id: RCV000059146 RCV001388583 RCV001813754 RCV002498349
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Arg300His
CA219364
NM_001164277.2:c.899G>A