Canonical Allele Identifier: PA219339
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68286
ClinVar RCV Id: RCV000059137 RCV000699431 RCV002504976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Gly20Asp
CA219337
NM_001164277.2:c.59G>A