Canonical Allele Identifier: PA2825972130
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2181223
ClinVar RCV Id: RCV002606034
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Met193Val
CA382900558
NM_001164279.2:c.577A>G