Canonical Allele Identifier: PA658832771
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 556518
ClinVar RCV Id: RCV000672537
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157749.1:p.Leu293Met
CA382898184
NM_001164277.2:c.877C>A