Canonical Allele Identifier: PA2825971894
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 3234897
ClinVar RCV Id: RCV004547245
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Gly372Val
CA382895883
NM_001164278.2:c.1115G>T