Canonical Allele Identifier: PA2825971679
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 556291
ClinVar RCV Id: RCV000672284
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ala170Thr
CA382902708
NM_001164278.2:c.508G>A