Canonical Allele Identifier: PA2825972239
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 550838
ClinVar RCV Id: RCV000665696
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Ile279Thr
CA382895854
NM_001164279.2:c.836T>C