Canonical Allele Identifier: PA2825971872
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 550942
ClinVar RCV Id: RCV000665846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Val320Ile
CA382897335
NM_001164278.2:c.958G>A