Canonical Allele Identifier: PA284851
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 6921
ClinVar RCV Id: RCV000007330 RCV000059116
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Gly339Cys
CA284849
NM_001164277.2:c.1015G>T