Canonical Allele Identifier: PA2825971082
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 965218

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Val34Ile
CA6311914
NM_001164277.2:c.100G>A