Canonical Allele Identifier: PA2825971202
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1965317
ClinVar RCV Id: RCV002726715

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Ile158Thr
CA382903150
NM_001164277.2:c.473T>C