Canonical Allele Identifier: PA2825971858
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 555977
ClinVar RCV Id: RCV000671902
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Val313Met
CA382897602
NM_001164278.2:c.937G>A