Canonical Allele Identifier: PA2741884917
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2769665
ClinVar RCV Id: RCV003507901
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Arg77Gly
CA382905862
NM_001467.6:c.229C>G