Canonical Allele Identifier: PA915985508
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 557547
ClinVar RCV Id: RCV000673703
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001458.1:p.Val228Met
CA229598307
NM_001467.6:c.682G>A