Canonical Allele Identifier: PA915988051
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 551352
ClinVar RCV Id: RCV000666390
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ala369Thr
CA382896005
NM_001164278.2:c.1105G>A