Canonical Allele Identifier: PA915988200
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_001157751.1:p.Gly77Arg
CA219322
NM_001164279.2:c.229G>A
CA382903471
NM_001164279.2:c.229G>C