Canonical Allele Identifier: PA2825971871
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350835
ClinVar RCV Id: RCV002042166
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Arg319Pro
CA382897341
NM_001164278.2:c.956G>C