Canonical Allele Identifier: PA2573185899
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1411318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Glu451Asp
CA382893109
NM_001164278.2:c.1353G>T
CA382893118
NM_001164278.2:c.1353G>C