Canonical Allele Identifier: PA1139690782
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 942276
ClinVar RCV Id: RCV001212230
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ile374Val
CA382895862
NM_001164278.2:c.1120A>G