Canonical Allele Identifier: PA2829335304
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 199062

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Ser356Thr
CA203733
NM_001467.6:c.1067G>C