Canonical Allele Identifier: PA658832765
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 554262
ClinVar RCV Id: RCV000669863
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Val275Ile
CA382900314
NM_001164277.2:c.823G>A