Canonical Allele Identifier: PA915988040
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 215175

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Phe360Leu
CA322806
NM_001164278.2:c.1078T>C
CA382896291
NM_001164278.2:c.1080T>G
CA382896292
NM_001164278.2:c.1080T>A