Canonical Allele Identifier: PA2825971824
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 555360
ClinVar RCV Id: RCV000671170

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Lys290Asn
CA382899881
NM_001164278.2:c.870G>T
CA382899882
NM_001164278.2:c.870G>C