Canonical Allele Identifier: PA2825971564
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551501
ClinVar RCV Id: RCV000666579
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Phe80Leu
CA382905737
NM_001164278.2:c.240C>G
CA382905738
NM_001164278.2:c.240C>A
CA382905747
NM_001164278.2:c.238T>C