Canonical Allele Identifier: PA915988030
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 554795
ClinVar RCV Id: RCV000670487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Leu351Ile
CA382896467
NM_001164278.2:c.1051C>A