Canonical Allele Identifier: PA915985668
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 555977
ClinVar RCV Id: RCV000671902
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Val313Met
CA382897602
NM_001467.6:c.937G>A