Canonical Allele Identifier: PA2825971634
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 877114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Glu130Asp
CA382904157
NM_001164278.2:c.390G>T
CA382904163
NM_001164278.2:c.390G>C