Canonical Allele Identifier: PA915988089
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68269
ClinVar RCV Id: RCV000059119
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ala395Asp
CA219282
NM_001164278.2:c.1184C>A