Canonical Allele Identifier: PA2825972094
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1209841
ClinVar RCV Id: RCV001579268 RCV001579267
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Phe164Leu
CA382901269
NM_001164279.2:c.492T>G
CA382901271
NM_001164279.2:c.492T>A
CA382901293
NM_001164279.2:c.490T>C