Canonical Allele Identifier: PA2825971652
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 68279
ClinVar RCV Id: RCV000059130 RCV001390447
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Ala148Val
CA219316
NM_001164278.2:c.443C>T