Canonical Allele Identifier: PA2825971051
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044548
ClinVar RCV Id: RCV001348806 RCV002486432 RCV003405582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Gly5Arg
CA382909264
NM_001164277.2:c.13G>C