Canonical Allele Identifier: PA658676301
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 459625
ClinVar RCV Id: RCV000524561 RCV001547830 RCV002377036 RCV003935410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Ala291Val
CA6311694
NM_001164277.2:c.872C>T