Canonical Allele Identifier: PA2825972050
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2979970
ClinVar RCV Id: RCV003835080
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Asp127Tyr
CA382901964
NM_001164279.2:c.379G>T