Canonical Allele Identifier: PA1139705559
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 846325
ClinVar RCV Id: RCV001049603 RCV002481952
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Arg319Trp
CA6311681
NM_001467.6:c.955C>T