Canonical Allele Identifier: PA2580168852
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2074546
ClinVar RCV Id: RCV002976289
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Pro380Ser
CA6311634
NM_001164278.2:c.1138C>T