Canonical Allele Identifier: PA915988152
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 652090
ClinVar RCV Id: RCV000807579 RCV002271588 RCV002281135 RCV002507401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Glu451Ala
CA6311575
NM_001164278.2:c.1352A>C