Canonical Allele Identifier: PA2825971810
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557457
ClinVar RCV Id: RCV000673600

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Gly276Ala
CA382900260
NM_001164278.2:c.827G>C