Canonical Allele Identifier: PA2825971815
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 288246
ClinVar RCV Id: RCV000319235 RCV002518026
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ala280Val
CA6311720
NM_001164278.2:c.839C>T