Canonical Allele Identifier: PA2499258209
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1037192
ClinVar RCV Id: RCV001340308
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Gly247Asp
CA382901060
NM_001467.6:c.740G>A