Canonical Allele Identifier: PA2825971808
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397113
ClinVar RCV Id: RCV001887568

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Val275Gly
CA382900287
NM_001164278.2:c.824T>G