Canonical Allele Identifier: PA2825971839
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1765207

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Asn298Lys
CA382898024
NM_001164278.2:c.894C>G
CA382898027
NM_001164278.2:c.894C>A