Canonical Allele Identifier: PA2499240378
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1011254
ClinVar RCV Id: RCV001309019
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ser363Phe
CA382896196
NM_001164278.2:c.1088C>T