Canonical Allele Identifier: PA2825971261
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1445899
ClinVar RCV Id: RCV001985296

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Gln218Arg
CA382901568
NM_001164277.2:c.653A>G