Canonical Allele Identifier: PA2825971059
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1512595
ClinVar RCV Id: RCV002045690
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Thr11Pro
CA382909038
NM_001164277.2:c.31A>C