Canonical Allele Identifier: PA915985135
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 552003
ClinVar RCV Id: RCV000667188

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Ala2Thr
CA382909340
NM_001467.6:c.4G>A