Canonical Allele Identifier: PA219330
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68283
ClinVar RCV Id: RCV000059134
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Cys176Arg
CA219328
NM_001164277.2:c.526T>C