Canonical Allele Identifier: PA2825972057
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2897501
ClinVar RCV Id: RCV003618890

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Glu132Lys
CA382901875
NM_001164279.2:c.394G>A