Canonical Allele Identifier: PA2825971079
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2172207
ClinVar RCV Id: RCV003087309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Thr30Ile
CA382908448
NM_001164277.2:c.89C>T