Canonical Allele Identifier: PA915985141
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557159
ClinVar RCV Id: RCV000673263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Ser15Leu
CA382908911
NM_001467.6:c.44C>T