Canonical Allele Identifier: PA2825971476
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 580779
ClinVar RCV Id: RCV000704424

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Phe26Leu
CA382908541
NM_001164278.2:c.78C>G
CA382908544
NM_001164278.2:c.78C>A
CA382908571
NM_001164278.2:c.76T>C