Canonical Allele Identifier: PA2825971655
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68281
ClinVar RCV Id: RCV000059132 RCV000794844 RCV002483116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Gly150Arg
CA219322
NM_001164278.2:c.448G>A
CA382903471
NM_001164278.2:c.448G>C