Canonical Allele Identifier: PA2825971835
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 553652
ClinVar RCV Id: RCV000669148
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157750.1:p.Tyr296Asp
CA229597269
NM_001164278.2:c.886T>G