Canonical Allele Identifier: PA2825971440
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1411318
ClinVar RCV Id: RCV001942933 RCV002478373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Glu429Asp
CA382893109
NM_001164277.2:c.1287G>T
CA382893118
NM_001164277.2:c.1287G>C