Canonical Allele Identifier: PA915988037
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 550787
ClinVar RCV Id: RCV000665629
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Val355Leu
CA382896394
NM_001164278.2:c.1063G>T
CA382896397
NM_001164278.2:c.1063G>C