Canonical Allele Identifier: PA2825971274
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1209841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Phe237Leu
CA382901269
NM_001164277.2:c.711T>G
CA382901271
NM_001164277.2:c.711T>A
CA382901293
NM_001164277.2:c.709T>C