Canonical Allele Identifier: PA2825972184
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_001157751.1:p.Val240Met
CA382897602
NM_001164279.2:c.718G>A