Canonical Allele Identifier: PA658832754
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 552741
ClinVar RCV Id: RCV000668062 RCV002485543
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Trp227Arg
CA382901466
NM_001164277.2:c.679T>A
CA382901468
NM_001164277.2:c.679T>C