Canonical Allele Identifier: PA2825972135
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1397113
ClinVar RCV Id: RCV001887568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Val202Gly
CA382900287
NM_001164279.2:c.605T>G