Canonical Allele Identifier: PA2741839065
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2717939
ClinVar RCV Id: RCV003508380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Glu377Arg
CA2697552051
NM_001164278.2:c.1129_1130delinsAG