Canonical Allele Identifier: PA2825971312
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 969047
ClinVar RCV Id: RCV001244305 RCV003117861 RCV003166529
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Ala291Gly
CA6311695
NM_001164277.2:c.872C>G