Canonical Allele Identifier: PA2825972129
Gene: SLC37A4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2189722
ClinVar RCV Id: RCV002611772
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157751.1:p.Tyr192His
CA382900590
NM_001164279.2:c.574T>C