Canonical Allele Identifier: PA2825971724
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 574430
ClinVar RCV Id: RCV000696358
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Asp200Glu
CA382901951
NM_001164278.2:c.600C>G
CA382901952
NM_001164278.2:c.600C>A