Canonical Allele Identifier: PA2825971722
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468368
ClinVar RCV Id: RCV001993648

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Leu199Arg
CA382901973
NM_001164278.2:c.596T>G